Reported Feb 25, 2015 · Terminated
Ringloc+ Acetabular Shell Finned 52 mm, PN 16-104152, hip prosthesis component.
Biomet, Inc.
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: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
Ringloc+ Acetabular Shell Finned 52 mmPN 16-104152hip prosthesis component
- Lot codes and dates
- Catalog Number16-104152
- Lot Number Identification427840
- Amount recalled
- 17
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Biomet recalled the Mallory Head 4 Finned Acetabular Shell 50mm (Lot 364600) and Ringloc + Acetabular Shell Limited Hole Finned 52 mm (Lot 427840) following a mix up in packaging with the two.
This product could cause temporary or reversible health problems — stop using it.
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