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

Recall Z-0679-2022 — The DARCO¿ Locking Bone Plate System is designed with rhombus (parallelogram) plates of biocompatible titanium. The plates use either 2.7mm or 3.5mm screws which intersect each other in pairs. The drill holes of the plates are aligned to assure the screws do not touch. The various plates model nu

U.S. FDA — Device Enforcement · United States · 2022-02-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0679-2022
Date of alert: 2022-02-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Wright Medical Technology, Inc.
Product category: device
Product type: Devices

Reported risk: Product was labelled with the incorrect manufacturing and distribution dates.

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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