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

Recall Z-0829-2014 — AnspacSingle use Sterile bone cutting burs.h REF: S-1504TD Twist Drill for 1.5mm x 4mm screw. Rx only Single use Sterile bone cutting burs.

U.S. FDA — Device Enforcement · United States · 2011-03-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0829-2014
Date of alert
2011-03-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
The Anspach Effort, Inc.
Product category
device
Product type
Devices
Reported risk: Cutter was longer than was stated on the label
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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