Biomet, Inc. recalls Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
- Recall date
- January 7, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1208-2015
- FDA classification
- Class II
- Brand / firm
- Biomet, Inc.
- Sold / distributed
- Domestic: AL, FL, NY, TX Foreign: None
Why it was recalled
The taper adaptor is missing from the packaging, which may result in a delay in surgery greater than 30 minutes.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
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