OMNIlife science Inc. recalls

15 recalls on record · latest: December 21, 2020

Official U.S. recall history for OMNIlife science Inc., compiled from official government records.

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OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 49/28-ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup fo…

December 21, 2020 · Medical device recalls Moderate risk Acetabular Liners have a higher than acceptable oxidation limit, potential for…

OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup f…

December 21, 2020 · Medical device recalls Moderate risk Acetabular Liners have a higher than acceptable oxidation limit, potential for…

OMNIlife science Inc. recalls SERF Novae Dual Mobility Cup Insert 47/28- ApeX-LNK Poly Liner. Intended for use with the Apex Modular Acetabular Cup f…

December 21, 2020 · Medical device recalls Moderate risk Acetabular Liners have a higher than acceptable oxidation limit, potential for…

OMNIlife science Inc. recalls OMNI Hip System Model, Catalogue, or Order Number(s): HC-00070 Intended for use as the femoral component of a primary o…

September 11, 2019 · Medical device recalls Moderate risk Stems missing porous coating on the device.

OMNIlife science Inc. recalls OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Insert Liner 51-28; Produc…

July 23, 2019 · Medical device recalls Moderate risk Acetabular liners failed the oxidation testing performed prior to release. They…

OMNIlife science Inc. recalls OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component ApeX-LNK crosslinked Acetabular Insert, 10 deg ho…

July 23, 2019 · Medical device recalls Moderate risk Acetabular liners failed the oxidation testing performed prior to release. They…

OMNIlife science Inc. recalls OMNIlife science, Inc. ApeX acetabular liner hip prosthesis component Serf Dual Mobility Cup Liner 53-28; Product code:…

July 23, 2019 · Medical device recalls Moderate risk Acetabular liners failed the oxidation testing performed prior to release. They…

OMNIlife science Inc. recalls OMNIBotics iBlock Cutting Guide, 4146-1000 - Product Usage: The OMNIBotics iBlock Cutting Guide is a stainless-steel su…

April 12, 2019 · Medical device recalls Moderate risk The OMNIBotics iBlock Cutting Guide does not lock onto the iBlock Saw Guide as…

OMNIlife science Inc. recalls OMNI K1 Broach Handle, Product Code HS-10054

November 29, 2018 · Medical device recalls Moderate risk There is a potential for the inner pin of the handle to become loose and fall o…

OMNIlife science Inc. recalls OMNI Hip System, ApeX-LNK Acetabular Inserts 0 degree, 4+mm offset, Product Codes: H6-14436, H6-13928 & H6-14836 Produc…

May 18, 2018 · Medical device recalls Moderate risk The Internal packaging, the pouch and patient labels are improperly labeled.

OMNIlife science Inc. recalls Apex Knee System, Tibial Baseplate Size 6 Left, non-porous - KC-2206L The Apex Knee System is intended for use as a pri…

November 20, 2017 · Medical device recalls Moderate risk The Apex Knee System Tibial Baseplate identified has an improper expiration dat…

Omnilife Science Inc. recalls Offset Femoral Alignment Guide 4mm x 6¿; Product Code: KS 67024 Product Usage: The instrumentation has been designed to…

June 9, 2015 · Medical device recalls Moderate risk The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are incorr…

Omnilife Science Inc. recalls Offset Femoral Alignment Guide, 2mm x 6¿; Product Code: KS 67022 Product Usage: The instrumentation has been designed t…

June 9, 2015 · Medical device recalls Moderate risk The markings on both versions of the OFFSET FEMORAL ALIGNMENT GUIDES are incorr…

Omnilife Science Inc. recalls APEX INTERFACE Hemi 54X and Flared 56X, 3 Hole Acetabular Shells; Model: H5-12354, H5-11356. Product Usage: The Apex In…

June 4, 2015 · Medical device recalls Moderate risk The device may have improper screw hole placement due to inaccurate location of…

Omnilife Science Inc. recalls Apex ARC Hip Stem, HA Coated, Size 5; Product Code: HC-21005-HA Product Usage: The Apex ARC Hip Stem is the femoral com…

June 3, 2015 · Medical device recalls Moderate risk Product may breach the inner and outer sterile pouches during shipping or handl…