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CELL-DYN
ABBOTT LABORATORIES · Model 05H2901 · UDI-DI 00380740071899
GKJ
Prescription
6
510(k) clearances
105
Adverse events
1
Recalls
4
Facilities
Description
CELL-DYN Slide Maker Stainer
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2005-12-15 | Beckman Coulter Inc | There is a risk of sample misidentification when processing samples in the Manual aspiration mode. |
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
