CooperSurgical, Inc. recalls ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
- Recall date
- March 27, 2019
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1367-2019
- FDA classification
- Class II
- Brand / firm
- CooperSurgical, Inc.
- Sold / distributed
- Foreign: Denmark, Italy, Sweden
Why it was recalled
ICSI CUSTOM MICROPIPETTES the thirty-degree bend is absent
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
ICSI MICROPIPETTE CooperSurgical part number: MICC001-30-B1.0
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