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

Recall Z-0699-2024 — Medtronic, REF 9733236, Pin, 150mm, STERILE, PERCUTANEOUS

U.S. FDA — Device Enforcement · United States · 2023-11-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0699-2024
Date of alert
2023-11-28
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Navigation, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00613994247865
Reported risk: Their is the potential that the percutaneous pin may have a cross-pin that may render the pin unable to fit into tap cap, or too tight to remove.
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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