Z-1574-2014 Class II Terminated
FDA device recall Z-1574-2014 was initiated by The Anspach Effort, Inc. on Jan 8, 2014 and is designated Class II. Reason for recall: Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product. The recall status is terminated (terminated Jan 20, 2015). Affected quantity: 30 cutting burs affected.
Recall Details
- Product Type
- Devices
- Report Date
- May 21, 2014
- Initiation Date
- Jan 8, 2014
- Termination Date
- Jan 20, 2015
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 30 cutting burs affected
Product Description
ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length. REF L-3SD Use with LONG Attachments. Used for cutting and shaping bone, including the spine and cranium.
Reason for Recall
Anspach product code L-3SD contained product code S-3SD which is shorter in length than the labeled product.
Distribution Pattern
Nationwide Distribution including FL, TX, NC, IL, CO, and PA.
Code Information
Lot/Set/Serial: G323081803.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1574-2014
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026