Stryker Howmedica Osteonics Corp. recalls

52 recalls on record · latest: April 26, 2017

Official U.S. recall history for Stryker Howmedica Osteonics Corp., compiled from official government records.

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Stryker Howmedica Osteonics Corp. recalls Hoffmann LRF Safety Clip (Bone Transport Strut), 14 x 12 x 5 mm, REF 4933-0-401, NDC (01)07613327131475(10)V07241 Produ…

April 26, 2017 · Medical device recalls Moderate risk Stryker is recalling Hoffmann LRF (Limb Reconstruction Frame) System Safety Cli…

Stryker Howmedica Osteonics Corp. recalls Reunion TSA Peg Alignment Sound Catalog #5901-1038 The Peg Alignment Sound (PIN 5901-1038, Revision A) is an instrument…

December 2, 2016 · Medical device recalls Moderate risk Reunion TSA Peg Alignment Sound broke during surgery.

Stryker Howmedica Osteonics Corp. recalls GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1…

November 9, 2016 · Medical device recalls Moderate risk A review of packaging revealed the seal integrity of the pouch may be compromis…

Stryker Howmedica Osteonics Corp. recalls LFIT Anatomic V40 Femoral Head, Low Friction Ion Treatment, Sterile, 36 mm, REF 6260-9-236; Modular components designed…

August 29, 2016 · Medical device recalls Moderate risk Stryker received several complaints describing incidence of harm secondary to t…

Stryker Orthopaedics Universal Acetabular Cup Positioner/Impactor recalled over sterility concerns

August 18, 2016 · Medical device recalls Moderate risk Stryker Orthopaedics has received reports of the thread length protruding past…

Stryker Orthopaedics Patella Assembly Instrument recalled over sterility concerns

August 1, 2016 · Medical device recalls Moderate risk Upon failure of the press-fit, the clamping sub components and pins could disas…

Stryker Howmedica Osteonics Corp. recalls Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a reusable instrument which is part of the Exeter fe…

July 1, 2016 · Medical device recalls Moderate risk Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

Stryker Howmedica Osteonics Corp. recalls Supracondylar Nail T2 SCN 09x300 mm T2 Supracondylar Nail System is intended to provide strong and stable internal fixa…

June 30, 2016 · Medical device recalls Moderate risk Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled…

Stryker Howmedica Osteonics Corp. recalls Femoral Nail, A/R T2 Femur 011x280 mm T2 Femoral Nailing System is one of the first femoral nailing systems to offer an…

June 30, 2016 · Medical device recalls Moderate risk Stryker discovered that a Tibial Nail and femoral Nail were incorrectly labeled…

Stryker Howmedica Osteonics product recalled over sterility concerns

June 23, 2016 · Medical device recalls Moderate risk It was reported that the secondary locking mechanism, and its corresponding com…

Stryker Orthopaedics Modular Handle Triathlon Instruments recalled over sterility concerns

June 23, 2016 · Medical device recalls Moderate risk Stryker Orthopaedic is voluntarily recalling the Triathlon Modular Handle becau…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Trident Constrained Liner Inserter/Impactor Tip, 22 mm, 28 mm, and 32 mm. Non Sterile Catalog Numb…

June 3, 2016 · Medical device recalls Moderate risk Impactors do not meet the required sterility assurance level (SAL) of 10-6 when…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Smooth-Tipped, 3 x 800mm Product Usage: Intended for the temporary stabilization of bone segment…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, Gamma3 K-Wire with Washer, 13x3.2x500 mm Product Usage: Intended for the temporary stabilization of bone segme…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Ball-Tipped, 3 x 1000mm Product Usage: Intended for the temporary stabilization of bone segments…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Fixation K-Wire 3 x 285mm WCH coated Product Usage: Intended for the temporary stabilization of bone segmen…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Ball-Tipped, 2.5 x 1000mm Product Usage: Intended for the temporary stabilization of bone segmen…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Ball Tipped, 3 x 1250mm Product Usage: Intended for the temporary stabilization of bone segments…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Ball-Tipped, 3x800 mm Product Usage: Intended for the temporary stabilization of bone segments o…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 K-Wire, 3.2x400mm, CoCr, Recon Product Usage: Intended for the temporary stabilization of bone segments or…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 K-Wire 1.8 x 310 mm, Sterile Product Usage: Intended for the temporary stabilization of bone segments or fr…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, Gamma Guide Pin, 4x400 mm Product Usage: Intended for the temporary stabilization of bone segments or fragment…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 K-Wire, 3x285 mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Smooth-Tipped, 2.2 x 800mm Product Usage: Intended for the temporary stabilization of bone segme…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 Guidewire, Ball-Tipped, 2.5x800 mm Product Usage: Intended for the temporary stabilization of bone segments…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 K-Wire, 3.2x400mm, Recon Product Usage: Intended for the temporary stabilization of bone segments or fragme…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, METAIZEAU Intramedullary Pin, 2.0 x 400 mm Product Usage: Intended for the temporary stabilization of bone seg…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, Gamma K-Wire 3.2x450 mm, UNS-Thread Product Usage: Intended for the temporary stabilization of bone segments o…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, Gamma K-Wire 3.2x450 mm Product Usage: Intended for the temporary stabilization of bone segments or fragments.

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Howmedica Osteonics Corp. recalls Stryker, T2 K-Wire with washer, 7.8 x 3 x 285mm Product Usage: Intended for the temporary stabilization of bone segment…

January 21, 2016 · Medical device recalls Moderate risk During a review of the packaging, it was determined that the seal integrity of…

Stryker Vitallium Wire Non Sterile recalled over sterility concerns

December 23, 2015 · Medical device recalls Moderate risk The wire packages are correctly marked with a "NON-STERILE" label, however, the…

Stryker Howmedica Osteonics Corp. recalls Stryker PCA 10 Degree Hooded Acetabular Insert ID 22mm, Part of the Howmedica PCA Total Hip System intended for use dur…

October 15, 2015 · Medical device recalls Moderate risk Six (6) PCA 10 Degree Hooded Acetabular Insert-Duration 22 mm (ID) have been di…

Stryker Orthopaedics recalled over sterility concerns

September 29, 2015 · Medical device recalls Moderate risk Stryker is recalling various lots of the Trithion MIS Modular Distal Capture be…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Duracon Flat Tibial Wedge Cemented use only Sterile. Tibial Wedge is a component of Total Stabiliz…

September 21, 2015 · Medical device recalls Moderate risk Stryker Orthopaedics has received two customer complaints regarding Duracon Tib…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Tapers LFIT V40 Vitallium femoral heads. hip prosthesis component.

September 8, 2015 · Medical device recalls Moderate risk Complaints that the femoral head could not be assembled with its corresponding…

Stryker Howmedica Osteonics Corp. recalls Trident 10 degrees X3 Insert 36 mm ID Catalog #623-10-36I Hip implant component

June 25, 2015 · Medical device recalls Moderate risk it was discovered that item 623-10-36I Lot 3Y0KHP, although meeting all device…

Stryker Howmedica Osteonics Corp. recalls rHead Lateral Stem, Size 1, Do Not Reuse, Sterile. Intended for replacement of the proximal end of the radius.

June 24, 2015 · Medical device recalls Moderate risk Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum be…

Stryker Howmedica Osteonics Corp. recalls uHead, Ulnar Implant, Standard Stem, Size 1, Sterile, Rx Only. Intended for replacement of the distal radioulnar joint…

June 24, 2015 · Medical device recalls Moderate risk Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum be…

Stryker Howmedica Osteonics Corp. recalls Sigmoid Notch, Radial Plate, Small, Sterile, Do Not Reuse, Rx Only. Intended for replacement of the distal radio-ulnar…

June 24, 2015 · Medical device recalls Moderate risk Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum be…

Stryker Howmedica Osteonics Corp. recalls Recon, Radial Implant, Standard Stem, Size 1, Sterile, Do Not Reuse, Rx Only. Intended for replacement of the proximal…

June 24, 2015 · Medical device recalls Moderate risk Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum be…

Stryker Howmedica Osteonics Corp. recalls Radio-Capitellum, Capitellum, Left, Large, Do Not Reuse, Rx Only. Indicated for use in the elbow for reduction or relie…

June 24, 2015 · Medical device recalls Moderate risk Stryker is recalling rHead, uHead, Sigmoid Notch, Remotion, Radio Capitellum be…

Stryker Howmedica Osteonics Corp. recalls Triathlon PS X3 Tibial Insert; No. 3 Triathlon TS Plus Tibial Insert X3 Poly 19 mm Product Usage: The Triathlon PS X3 (…

May 29, 2015 · Medical device recalls Moderate risk Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS Plus…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Triathlon X3 Tibial Bearing Insert - CR REF 5530-G-209 (component of the Triathlon Total Knee Syst…

May 29, 2015 · Medical device recalls Moderate risk Stryker has received a report which identified that a Triathlon Tibial Bearing…

ReUnion TSA Shoulder System recalled over sterility concerns

May 12, 2015 · Medical device recalls Moderate risk A package labeled as Part #5901-S-4818, Lot MAC7C14, standard humeral head tria…

Stryker Howmedica Osteonics Corp. recalls Kinemax Stem Extenders, 80 mm, Product Usage: Kinemax Cemented Stem Extenders are modular components designed to be mat…

February 27, 2015 · Medical device recalls Moderate risk Stryker received four customer complaints reporting that inside the box labeled…

Stryker Howmedica Osteonics Corp. recalls Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon Distal Capture Assembly is used when a surgeon e…

February 12, 2015 · Medical device recalls Moderate risk Potential for weld disassociation of the cross pin, which could lead to loose o…

Stryker Howmedica Osteonics Corp. recalls LFT v40 Femoral Head; Catalog Number 6260-9-032; V40 CoCr LFit Head 32mm/-4. Designed to be assembled onto a femoral hi…

February 3, 2015 · Medical device recalls Moderate risk Three customer complaints were received for the same batch of V40 LFIT Vitalliu…

Stryker Howmedica Osteonics Corp. recalls Trident PSL HA Solid Back 50 mm Includes Dome Hole Plug Ref 540-11-50E Intended for cementless application in a total h…

December 15, 2014 · Medical device recalls Moderate risk Five customer complaints were received for the same batch of Trident PSL Shells…

Stryker Howmedica Osteonics Corp. recalls Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A subsidiary of Stryker C…

August 15, 2014 · Medical device recalls Moderate risk The peel strength of the inner blister may have been below internal validated r…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made i…

August 15, 2014 · Medical device recalls Moderate risk The peel strength of the inner blister may have been below internal validated r…

Stryker Howmedica Osteonics Corp. recalls Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp., A subsidiary of Stryker Corporation Made in…

August 15, 2014 · Medical device recalls Moderate risk The peel strength of the inner blister may have been below internal validated r…

Stryker Howmedica Osteonics Corp. recalls VariAx Compression Plating System

October 10, 2013 · Medical device recalls Moderate risk Stryker received two reports indicating that during screw insertion under a hig…