Z-1367-2019 Class II Terminated
FDA device recall Z-1367-2019 was initiated by CooperSurgical, Inc. on March 27, 2019 and is designated Class II. Reason for recall: ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent The recall status is terminated (terminated May 1, 2020). Affected quantity: 480 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 29, 2019
- Initiation Date
- March 27, 2019
- Termination Date
- May 1, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 480 units
Product Description
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
Reason for Recall
ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
Distribution Pattern
Foreign: Denmark, Italy, Sweden
Code Information
Lot 1557