Z-2839-2016 Class II Terminated
FDA device recall Z-2839-2016 was initiated by The Anspach Effort, Inc. on Aug 26, 2016 and is designated Class II. Reason for recall: The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503. The recall status is terminated (terminated Nov 29, 2017). Affected quantity: 63.
Recall Details
- Product Type
- Devices
- Report Date
- Sep 28, 2016
- Initiation Date
- Aug 26, 2016
- Termination Date
- Nov 29, 2017
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 63
Product Description
G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium.
Reason for Recall
The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
Distribution Pattern
AZ, DC, CA, MD, MI, and OR Switzerland
Code Information
Material M-3SB-2-G1 Batch J316017640
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2839-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026