FDA recall Z-1879-2018
CooperSurgical, Inc. · Class II · device
Product
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
Reason for recall
Products have been packaged with an incorrect product size.
Distribution
CA, SC, WI, MI, NH, MD, OH, NJ, Australia, France, Spain
Key facts
- Status
- Terminated
- Initiation date
- 2018-03-12
- Report date
- 2018-05-23
- Termination date
- 2019-05-08
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Trumbull, CT, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1879-2018