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

Recall Z-0631-2014 — Anspach BLACKMAX-N (Pneumatic motor) and Autolube III (Foot Control). Cutting and shaping bone.

U.S. FDA — Device Enforcement · United States · 2012-06-11 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0631-2014
Date of alert
2012-06-11
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
The Anspach Effort, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
50229989
Reported risk: Anspach was contacted by a hospital to inform Anspach that a Blackmax motor had been used in a case where the patient was diagnosed with Creutzfeldt-Jacob Disease (CJD).
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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