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

Recall Z-0626-2018 — G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for use in hip arthroplasty cases which involves the removal of the damaged joint and tissues to be replaced with artificial prosthesis. The result of the procedure is to relieve pain and restore a sense of normal function and mobility to the

U.S. FDA — Device Enforcement · United States · 2017-08-25 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0626-2018
Date of alert: 2017-08-25
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Biomet, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 110024464

Reported risk: The affected products are labeled and etched as F-44 mm liners; however, the physical products could potentially be E-42 mm liners.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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