Z-1879-2018 Class II Terminated
FDA device recall Z-1879-2018 was initiated by CooperSurgical, Inc. on Mar 12, 2018 and is designated Class II. Reason for recall: Products have been packaged with an incorrect product size. The recall status is terminated (terminated May 8, 2019). Affected quantity: 500.
Recall Details
- Product Type
- Devices
- Report Date
- May 23, 2018
- Initiation Date
- Mar 12, 2018
- Termination Date
- May 8, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 500
Product Description
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
Reason for Recall
Products have been packaged with an incorrect product size.
Distribution Pattern
CA, SC, WI, MI, NH, MD, OH, NJ, Australia, France, Spain
Code Information
Lot number: 212074
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1879-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 25, 2026