Zimmer Biomet, Inc. recalls DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
- Recall date
- June 30, 2017
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0992-2018
- FDA classification
- Class II
- Brand / firm
- Zimmer Biomet, Inc.
- Sold / distributed
- US in the state of Texas
Why it was recalled
Product may contain the presence of melted sterile packaging upon opening.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
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