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Zimmer Biomet, Inc. recalls DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Recalled March 21, 2018 · FDA recall Z-0992-2018 · Zimmer Biomet
Hazard
Product may contain the presence of melted sterile packaging upon opening. · FDA Class II
Units
30
Sold at
US in the state of Texas
Description
Product may contain the presence of melted sterile packaging upon opening.
Product
DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty
Manufacturer(s)
Zimmer Biomet, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →