Drug recall
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
FDA recall event 82663 · Class II · CooperSurgical, Inc.
Key facts
| Event ID | 82663 |
|---|---|
| Recall numbers | Z-1367-2019 |
| Recalling firm | CooperSurgical, Inc. |
| Product type | Devices |
| Products | ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent |
| Initiation date | Mar 27, 2019 |
| Report date | May 29, 2019 |
| Termination date | May 1, 2020 |
| City | Trumbull |
| State | CT |
| Country | United States |
| FEI number | 1216677 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: