Home / Recalls / Medical Devices
The Anspach Effort, Inc. recalls Anspach MIA 16 (16cm Minimally Invasive Attachment), Rx Only MIA16 attachments are intended for use with Motor System
Recalled January 22, 2014 · FDA recall Z-0779-2014 · The Anspach Effort
Hazard
Product did not reach expected sterility assurance level · FDA Class II
Units
183
Sold at
Nationwide Distribution: FL, IL, CA. IN, MI, CA, NJ, TX, NE, NC, OR, PA, TN, DC, UT, CO, MO, KY, MD, WV, NY, and MN.
Description
Product did not reach expected sterility assurance level
Product
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.
Manufacturer(s)
The Anspach Effort, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →