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LH Slidemaker
Beckman Coulter, Inc. · Model 6605633 · UDI-DI 15099590330620
GKJ
Prescription
6
510(k) clearances
105
Adverse events
1
Recalls
4
Facilities
Description
LH Slidemaker
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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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.