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

Recall Z-2548-2019 — QuickGraft¿ Model # 430PST

U.S. FDA — Device Enforcement · United States · 2019-08-15 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2548-2019
Date of alert
2019-08-15
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Musculoskeletal Transplant Foundation, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00319004921075
Reported risk: Measurement listed on the label is not taken under tension, and this would cause possible extension of surgical time needed to complete the procedure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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