ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1 — Class II medical device recall Z-1367-2019
Terminated recall by CooperSurgical, Inc., reported 2019-05-29. ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
| Recall number | Z-1367-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | CooperSurgical, Inc., Trumbull, CT, United States |
| Recall initiated | 2019-03-27 |
| Classified | 2019-05-17 |
| Reported by FDA | 2019-05-29 |
| Terminated | 2020-05-01 |
| Countries outside the US | DK, IT, SE |
| Quantity | 480 units |
| Lot numbers | 1557 |
| Model numbers | MICC001-30-B1.0 |
Product
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
Reason for recall
ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
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-1367-2019. 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.