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OMNIlife science Inc.

OMNIlife science Inc. Recalls

All product recalls associated with OMNIlife science Inc..

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Recall Summary

Total Recalls

Past Year

Class I (Serious)

Most Recent

Dec 2020

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1–3 of 3 recalls

OMNIlife science Inc.: SERF Novae Dual Mobility Cup Insert 51/28- ApeX-LNK Poly ...

Acetabular Liners have a higher than acceptable oxidation limit, potential for patients to experience a higher wear rate for acetabular liners and require a revision surgery

FDADec 21, 2020AL, ID, MD +2 more• OMNIlife science Inc.

OMNIlife science Inc.: OMNI Hip System Model, Catalogue, or Order Number(s): HC...

Stems missing porous coating on the device.

FDASep 11, 2019IL, OK• OMNIlife science Inc.

OMNIlife science Inc.: OMNIlife science, Inc. ApeX acetabular liner hip prost...

Acetabular liners failed the oxidation testing performed prior to release. They may experience a higher wear rate, leading to revision surgery.

FDAJul 23, 2019Nationwide• OMNIlife science Inc.