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

Recall Z-2797-2020 — Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wire

U.S. FDA — Device Enforcement · United States · 2020-07-28 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2797-2020
Date of alert: 2020-07-28
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Wright Medical Technology, Inc.
Product category: device
Product type: Devices

Reported risk: Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.

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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