FDA Device recall Z-1367-2019
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
- FDA Device
- Class II
- terminated
- Published 2019-05-29
On 2019-05-29 the FDA classified a Class II recall of ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0 by Coopersurgical, citing ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1367-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-27 |
| Published | 2019-05-29 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Coopersurgical |
| Distribution | n/a |
Product
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
Reason
ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
Identifiers
| code_info | Lot 1557 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1367-2019%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.