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All product recalls associated with Stryker Howmedica Osteonics Corp..
Total Recalls
1000
Past Year
353
Class I (Serious)
22
Most Recent
Jan 2026
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.
Stryker became aware that Catalog number 1594-1130S, Lot Code K559623 was manufactured with a lag screw hold angulation of 135 degrees rather than 130 degrees.
GE Healthcare received reports of intermittent low ejection fraction (EF) results for MUGA (multi-gated acquisitions) studies on Millennium VG systems. This issue can occasionally lead to distortions in the volume curve in some MUGA studies, and result in calculated EF values lower (never higher) than actual values. A low EF value could lead to a physician decision to stop needed treatment.
The recall includes Oceanic-brand Reliant BC inflators and AERIS-brand AW3 BC inflators. The Oceanic Reliant-type inflators have three flow-through holes in the hand grip of the lower inflator mechanism. The AERIS AW3 inflator has one flow-through hole in the hand grip of the lower inflator mechanism.