FDA Medical Device Recalls (openFDA)
CooperSurgical, Inc.: ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
- Recall number
- Z-1367-2019
- Recalling firm
- CooperSurgical, Inc.
- Product
- ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
- Status
- Terminated
- Initiated
- 2019-03-27
- Posted
- not on file
- Terminated
- 2020-05-01
- Reason
- ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
- Root cause
- Under Investigation by firm
- Action
- CooperSurgical issued recall letter dated March 27, 2019 identified problem and action to take: discontinue use of this discrepant product, quarantine the product, and complete the Acknowledgement and Receipt Form to arrange for either a product replacement or credit to your account through CooperSurgical. Contact: 203-601-5200 ext. 3300.
- Quantity
- 480 units
- Distribution
- Foreign: Denmark, Italy, Sweden
- Lot, serial or model codes
- Lot 1557
- 510(k) numbers
- ["K990847"]
- PMA numbers
- not on file
- Product code
- MQH
- Firm FEI
- 1216677
- Firm city
- Trumbull
- Firm state
- CT
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28