Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1035-2014 — MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID

U.S. FDA — Device Enforcement · United States · 2013-10-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1035-2014
Date of alert
2013-10-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Zimmer, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
60169597
Reported risk: Zimmer recently conducted a review of all historic packaging validations at its Zimmer Manufacturing B.V. (ZMBV) facility in Ponce, Puerto Rico. Based on this review, it was determined that the packaging operations conducted in the Building 1 packaging operation at this facility were not properly validated. As a result, Zimmer conducted seal integrity testing to evaluate if previously packaged product from this facility met the established requirements for sterile barrier integrity. The acceptance criteria established for this testing was 99% reliability with a 90% confidence interval. These packaging tray configurations met the acceptance criteria for sterile barrier integrity of both the inner and outer trays, however, Zimmer has decided to recall all manufacturing lots that have not expired and that were sterile packaged in the ZMBV facility Building 1 packaging operations.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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