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

Recall Z-0779-2014 — Anspach MIA 16 (16cm Minimally Invasive Attachment), Rx Only MIA16 attachments are intended for use with Motor Systems for cutting and shaping bones, including the spine and cranium.

U.S. FDA — Device Enforcement · United States · 2013-05-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0779-2014
Date of alert
2013-05-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
The Anspach Effort, Inc.
Product category
device
Product type
Devices
Reported risk: Product did not reach expected sterility assurance level
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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