Reported Dec 20, 2023 · Ongoing
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Encore Medical, LP
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Encore Medical, LP · 9800 Metric Blvd · Austin, TX · 78758-5445
Is this the product you have?
- RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
- Lot codes and dates
- Part Number508-32-204
- UDI-DI Code00888912144391
- Serial Numbers
769P2825769P2846769P2893
- Amount recalled
- 146 units
Where it was sold
Why it was recalled
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
This product could cause temporary or reversible health problems — stop using it.
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