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

Recall Z-0914-2022 — Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical instrument

U.S. FDA — Device Enforcement · United States · 2022-02-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0914-2022
Date of alert
2022-02-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Nextremity Solutions
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00817701020837
Reported risk: Proximal end of the driver is oversized in varying degrees, making it difficult to fully connect with and remove from the proximal Nextra implant, causing delay in surgery
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.

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