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

Recall Z-1924-2020 — WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.

U.S. FDA — Device Enforcement · United States · 2020-04-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1924-2020
Date of alert: 2020-04-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Wright Medical Technology Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 2000252902

Reported risk: One lot of INBONE Tibial Trays is missing the plasma coating.

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.

Recall Z-1924-2020 — WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.

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