Zimmer Manufacturing B.V. recalls

88 recalls on record · latest: May 4, 2016

Official U.S. recall history for Zimmer Manufacturing B.V., compiled from official government records.

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Zimmer Manufacturing B.V. recalls VersaFx Femoral Fixation System Hex head compression screw 4.7 mm dia. 2 inch (51 mm) length 47116202400

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls ITST intertrochanteric/subtrochanteric fixation 4.5 mm diameter cortical screw, 3.5 mm hex head, 57 mm length 002253057…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Trilogy self-tapping bone screw Bone screw 4.5x25 selftap 00625004525 Bone screw 4.5x50 selftap 00625004550 Bone screw…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls M/DN Intramedullary Fixation 4.2 mm Diameter Cortical Screw, 3.5 mm Hex Head, 45 mm Length 00225304542 M/DN Intramedull…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 4.0 mm Cancellous Screw Fully Threaded, 12 mm Length 47484001200 4.0 mm Cancellous Screw…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Zimmer universal locking system (ULS) 3.5 mm cortical screw selftapping 18 mm length 47493501801

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Hgp ii acetabular cup bone screw selftap 6.5x15mm 00662406515 Hgp ii acetabular cup bone screw selftap 6.5x20mm 0066240…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 2.7 mm Cortical Screw SelfTapping, 14 mm Length 47482701401

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Herbert Cannulated Bone Screw System, Bone Screw, 6.5 mm Dia., 45 mm Length 47115504507 Herbert Cannulated Bone Screw S…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Zimmer Plates and Screws (ZPS) 3.5 mm Cortical Screw SelfTapping, 10 mm Length 47483501001 3.5 mm Cortical Screw SelfTa…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Mini MagnaFx Cannulated Screw Fixation System Small Cannulated Bone Screw, Fully Threaded, 5.0 mm Diameter, 20 mm Lengt…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Periarticular plating system, cancellous bone screw, partially threaded, hex head, 4.0 mm diameter, 16 mm length 472347…

May 4, 2016 · Medical device recalls Moderate risk A small hole may be present in the inner tray of specific lots of sterile Hip a…

Zimmer Manufacturing B.V. recalls Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in t…

March 17, 2016 · Medical device recalls Moderate risk The firm received a customer complaint establishing that the product (Persona P…

Zimmer Manufacturing B.V. recalls Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 18mm Sterile For use in to…

March 17, 2016 · Medical device recalls Moderate risk The firm received a customer complaint establishing that the product (Persona P…

Zimmer Manufacturing B.V. recalls Product 25 consists of all product under product code: LPH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 48 consists of all product under product code: JWH and same usage: Item no: 597206526 NEXGEN ALL-POLY PATELLA,…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 12 consists of all product under product code JDI , and same usage: Item no: 902602935 6 DEGREE COCR FEM HEAD 2…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 31 consists of all product under product code: KTT and same usage: Item no: 118113003 FREE-LOCK TUBE & SCP PLAT…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 29 consists of all product under product code: LPHand same usage: Item no: 32902603800 FEMORAL HEAD +0.5 X 22 M…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 52 consists of product code: HWC and same usage: Item no: 525004530 NEXGEN OSTEOTOMY CORT BON 525004540 NEXGEN…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 18 consists of all product under product code: HWC and same usage: Item no: 47248001441 CANC SCR 4.0MM X 14MM F…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 5 consists of all products under product code HWC, and same usage: Item no: 47482701001 2.7MM CORT. SCREW 10MM,…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 28 consists of all product under product code: JDI and same usage: Item no: 32902605000 FEMORAL HD 28MM MEDIUM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 51 consists of all product under product code: JWH and same usage: Item no: 598603701 NEXGEN OPTION STEMMED TIB…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 36 consists of all product under product code: HSB and same usage: Item no: 225302745 INTERLOCKING IM SCREW 4.5…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 17 consists of all product under product code: LPH and same usage: Item no: 625004515 BONE SCREW 4.5X15 SELF-TA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 45 consists of all product under product code: JWH and same usage: Item no: 511007020 MGII KNEE SLF-TAP BONE ST…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 34 consists of all product under product code: JWH and same usage: Item no: 522001700 I/B II KNEE DOMED PATELLA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 59 consists of all product under product code: JWH and same usage: Item no: 42540000026 PSN ALL POLY PAT PLY 26…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 10consists of all product under product code HWC, and same usage: Item no: 47484502601 4.5 X 26 CORT SCREW SELF…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 65 consists of all product under product code: KTT and same usage: Item no: 119413594 VERSA-FX II KEYLESS SHORT…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 14 consists of all product under product code HSB , and same usage: Item no: 225600230 ASIA ONE-PIECE LAG SCREW…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 62 consists of all product under product code: LPH and same usage: Item no: 620003620 TRILOGY ACET SHELL 36MM O…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 19 consists of all product code: JDI and same usage: Item no: 765301101 CEM FEM ST 11X120 NOCOAT 765301201 CEM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 35 consists of all product under product code: JWH and same usage: Item no: 522007300 I/B II KNEE FLUTED ROD, 1…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 67 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 54 consists of all product under product code: JWH and same usage: Item no: 596009900 NEXGEN TAPER PLUG for use…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 1 consists of all product under , product code: JWH and same usage: Item no: 47481500601 1.5 X 6 CORT SCREW HEX…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 64 consists of all product under product code: JDI and same usage: Item no: 902605101 UNIPOLAR ENDO FEM HEAD 51…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 37 consists of all product under product code: HSB and same usage: Item no: 225302055 INTERLOCKING IM SCREW LG…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 27 consists of all product under product code: HSB and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 7 consists of all products under product code HWC, and same usage: Item no: 47234801435 3.5MM CORT SCR X 14MM 4…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 8 consists of all products under product code HWC, and same usage: Item no: 47483501201 3.5MM CORT. SCREW 12MM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 3 consists of all products under product code JDI, and same usage: Item no:781803800 12/14 UNIPOLAR FEMORAL HE…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 15 consists of all product code JDI , and same usage: Item no: 805002802 ASTEL FEM HEAD +0X28MM DI 805002805 AS…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 56 consists of all product under product code: HWC and same usage: Item no: 47234702032 PERI SCR 3.5MM X 32MM S…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 42 consists of all product under product code: HSB and same usage: Item no: 225224010 M/DN FEM IM NAIL 10MM DIA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 43 consists of all product under product code: HSB and same usage: Item no: 224001016 M/DN R-F IM NAIL 10MM DIA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 4 consists of all products under product code HWC, and same usage: Item no: 47482002603 2.0 X 26 CORT SCREW CRU…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 16 consists of all product under poduct code: KWY and same usage: Item no: 500103822 BIPOLAR LINER 38MM OD X 2…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 46 consists of all product under product code: HWC and same usage: Item no: 114204012 MINI MAGNA-FX CANN SCREW…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 69 consists of all product under product code: JDI and same usage: Item no: 785301701 VERSYS CEMENTED FEM STEM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 30 consists of all product under product code: KTT and same usage: Item no: 118100527 FREE-LOCK LAG SCREW, 12.7…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 60 consists of all product under product code: HSB and same usage: Item no: 225207055 RECON SCREW LG 5.5MM DIA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 53 consists of all product under: product code: JWH and same usage: Item no: 597002501 NEXGEN PRECOAT PEG TIB P…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 63 consists of all product under product code: LPH and same usage: Item no: 620004020 TRILOGY ACET SHELL 40MM O…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 70 consists of all product under product code: JDI and same usage: Item no: 785701000 VERSYS HERITAGE FEM STEM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 66 consists of all product under product code: JDI and same usage: Item no: 785001100 VERSYS ADVOCATE CEMENTED…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 20 consists of all prod oct under poduct code: KTT and same usage: Item no: 47116201900 COMPRESSION SCREW 1/2IN…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 22 consists of all product under product code: JDI and same usage: Item no: 811400218 CPT 12/14 COCR REVISION S…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 13 consists of all product under product code HWC , and same usage: Item no: 47486510002 6.5 X 100 CANC SCREW,…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 71 consists of all product under product code: JDI and same usage: Item no: 783401000 VERSYS PRESS FIT LD/FX ST…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 40 consists of all product under product code: HSB and same usage: Item no: 225706565 ITST ANTI-ROTATION SCREW…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 47 consists of all product under product code: LPH and same usage: Item no: 611004022 MODULAR CUP 10 DEGREE LIN…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 49 consists of all product under product code: JWH and same usage: Item no: 597206529 NEXGEN ALL-POLY PATELLA,…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 26 consists of all product under product code: JWH and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 41 consists of all product under product code: KTT and same usage: Item no: 119301042 LAG SCR 12.7D X 100MM STA…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 32 consists of all product under product code: HWC and same usage: Item no: 47115401200 HERBERT BONE SCREW, 3.0…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 9 consists of all product under HRS, and same usage: Item no: 47494502601 4.5 BROAD SCP PLT, 26 HOL Product Usa…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 50 consists of all product under product code: JWH and same usage: Item no: 595002701 NEXGEN MIS TIBIA PLATE PR…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 39 consists of all product under product code: JDI and same usage: Item no: 32902605800 ION IMPLANTED FEM 22MM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 57 consists of all product code: JDI and same usage: Item no: 763401000 PRESSFIT FEM ST FX 10 X 115 763401100 P…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 11 consists of all product under product code JDI , and same usage: Item no: 902602500 6 DEGREE COCR FEM HEAD 2…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 33 consists of all product under product code: JDI and same usage: Item no: 662406515 HGP II ACETABULAR CUP BON…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 38 consists of all product under product code: HSB and same usage: Item no: 225303255 INTERLOCKING IM SCREW LG…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 58 consists of all product under product code: HRS and same usage: Item no: 234800904 PROXIMAL DORSAL ULNA PLT…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 55 consists of all product under product code: HSB and same usage: Item no: 225900132 ONE-PIECE LAG SCREW 11MM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 6 consists of all products under product code HWC, and same usage: Item no: 47493501001 3.5 X 10 CORT SCREW SEL…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 2 consists of all products product code LPH, and same usage: 801802202 12/14 COCR FEMORAL HEAD 2 801802220 12/1…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 61 consists of all product under product code: JWH and same usage: Item no: 598003712 STD PRECOAT TIBIA PLATE S…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 68 consists of all product under product code: JDI and same usage: Item no: 787101360 VERSYS CEM/REV/CALCAR 13X…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 21 consists of all product under product code: JDI and same usage: Item no: 811400218 CPT 12/14 COCR REVISION S…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 23 consists of all product code: JDI and same usage: Item no: 801100220 CPT 2 HIP STEM, X-OFFSET 801100320 CPT…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 44 consists of all product under product code: HWC and same usage: Item no: 114607099 MAGMA-FX CANN SCREW 7.0MM…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 24 consists of all product under product code: HRS and same usage: Item no: 234703104 DISTAL MEDIAL FEMORAL CON…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls Product 72 consists of all product code: JDI and same usage: Item no: 805002202 ZIMTRON HEAD 12/14 0X22 MM For use in t…

January 11, 2016 · Medical device recalls Moderate risk As a result of the insufficient sealer calibration data for product packaged in…

Zimmer Manufacturing B.V. recalls NexGEN System REF 5980-37-01 Tibial Component Size Stemmed 3 Precoat, and REF 5986-37-01 Nonaugmentable Tibial Componen…

December 3, 2015 · Medical device recalls Moderate risk A product complaint was received stating that a carton labeled as a Precoat Ste…

Zimmer Manufacturing B.V. recalls Label reading in part as: "NexGen System, Complete Knee Solution; Reference Number 5980-37-01; Tibial Component, Precoa…

December 2, 2015 · Medical device recalls Moderate risk Complaints were received from Thailand reporting that there was no white paper…