Z-0779-2014 Class II Terminated
FDA device recall Z-0779-2014 was initiated by The Anspach Effort, Inc. on May 6, 2013 and is designated Class II. Reason for recall: Product did not reach expected sterility assurance level The recall status is terminated (terminated Apr 18, 2016). Affected quantity: 183.
Recall Details
- Product Type
- Devices
- Report Date
- Jan 22, 2014
- Initiation Date
- May 6, 2013
- Termination Date
- Apr 18, 2016
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 183
Product Description
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.
Reason for Recall
Product did not reach expected sterility assurance level
Distribution Pattern
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.
Code Information
ALL LOTS
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0779-2014
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026