Biomet, Inc. recalls Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
- Recall date
- July 28, 2015
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2483-2015
- FDA classification
- Class II
- Brand / firm
- Biomet, Inc.
- Sold / distributed
- Distributed in Canada and Japan.
Why it was recalled
The device was assembled without screw hole plugs.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Vision RingLoc Shell 50 mm Size 23. Hip joint replacement prosthesis.
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