FDA Device recall Z-1879-2018
Fischer Cone Biopsy Excisor, Medium (5/Box)
- FDA Device
- Class II
- terminated
- Published 2018-05-23
On 2018-05-23 the FDA classified a Class II recall of Fischer Cone Biopsy Excisor, Medium (5/Box) by Coopersurgical, citing products have been packaged with an incorrect product size.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1879-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-12 |
| Published | 2018-05-23 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Coopersurgical |
| Distribution | CA, MD, MI, NH, NJ, OH, SC, WI |
Product
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
Reason
Products have been packaged with an incorrect product size.
Identifiers
| code_info | Lot number: 212074 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1879-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.