Z-2837-2016 Class II Terminated
FDA device recall Z-2837-2016 was initiated by The Anspach Effort, Inc. on Aug 26, 2016 and is designated Class II. Reason for recall: Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed. The recall status is terminated (terminated Nov 29, 2017). Affected quantity: 177.
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
- 177
Product Description
G1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.
Reason for Recall
Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed.
Distribution Pattern
AZ, DC, CA, MD, MI, and OR Switzerland
Code Information
Material L-7B-G1 Batch K043113667
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2837-2016
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026