Official recall record

SCORPIO RECESSED METAL BACKED PATELLA 3045-0026 3045-0028 3045-0030 3045-0032 Orthopaedic implant components manufactured fro

US FDA — Medical Devices · 2026-07-30 · United StatesClass II

Issuing authority: US FDA — Medical Devices
Recall initiated by firm: 2026-07-30
Country of alert: United States
Alert level: Class II
Alert type: recall
Brand on record: Howmedica Osteonics Corp.

What the authority reported

Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels of oxidation, which may result in increased wear, leading to hazards such as excessive wear debris, material fragments, fractured device, or disassociated device. Potential harms include revision surgery, pain, and inflammation.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-10-15.

More recalls: US FDA — Medical Devices · United States · all filters

Other recalls from this brand

2026-09-16 · US FDA — Medical Devices
TS Femoral Prep Tray, Triathlon. Catalog Number: 6543-6-507.
2026-09-16 · US FDA — Medical Devices
TS Misc. Instruments Tray, Triathlon. Catalog Number: 6543-6-519.
2026-09-16 · US FDA — Medical Devices
Triathlon Hinge Femoral Prep Tray. Catalog Number: 6543-6-514.

All 20 official recall notices naming Howmedica Osteonics Corp. on this site →

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.