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

Recall Z-2158-2013 — Steinmann Pin, packed in a clear tube with end caps, tubes packed in a sterile barrier pouch, 6 pouches/sales unit. Pouches are labeled in part ***MicroAire Surgical Instruments 3590 Grand Forks Blvd Charlottesville, VA LLC 22911*** Models: 1620-109 1636-509 1620-509 1

U.S. FDA — Device Enforcement · United States · 2013-08-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2158-2013
Date of alert
2013-08-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MicroAire Surgical Instruments, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
0213216244
Reported risk: A medical device used in surgical procedures was packaged in a pouch in which a defective seal may compromise sterility
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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