Class II — CooperSurgical, Inc.
| Recalling firm | COOPERSURGICAL, INC. |
|---|---|
| Registered facility | View this company's 6 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent |
| Product | ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0 |
| Quantity | 480 units |
| Distribution | Foreign: Denmark, Italy, Sweden |
| Initiated | 2019-03-27 |
| Classified | 2019-05-17 |
| Terminated | 2020-05-01 |
| Recall number | Z-1367-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — CooperSurgical, Inc. (Z-1367-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82663/
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