Fischer Cone Biopsy Excisor — Class II medical device recall Z-1879-2018
Terminated recall by CooperSurgical, Inc., reported 2018-05-23, distributed in CA, MD, MI, NH, NJ, OH, SC, WI. Products have been packaged with an incorrect product size.
| Recall number | Z-1879-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2018-03-12 |
| Classified | 2018-05-15 |
| Reported by FDA | 2018-05-23 |
| Terminated | 2019-05-08 |
| Distributed | CA, MD, MI, NH, NJ, OH, SC, WI |
| Countries outside the US | AU, ES, FR |
| Quantity | 500 |
| Lot numbers | 212074 |
| Model numbers | 900-151 |
Product
Fischer Cone Biopsy Excisor, Medium (5/Box); Model Number: 900-151
Reason for recall
Products have been packaged with an incorrect product size.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1879-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.