Home › Beckman Coulter, Inc. › Ac•T Rinse Shutdown Diluent
Ac•T Rinse Shutdown Diluent
Beckman Coulter, Inc. · Model 8547113 · UDI-DI 15099590625825
JCB
Prescription
0
510(k) clearances
31
Adverse events
3
Recalls
44
Facilities
Description
Ac•T Rinse Shutdown Diluent (500 ml)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-08-29 | Microcare Medical | Contaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter asburiae, Enterobacter bugandensis, pathogenic and opportunistic bacteria, to occur in ultrasonic deter |
| 2013-11-08 | Beckman Coulter Inc. | Beckman Coulter is recalling the UniCel DxH800 and UniCel DxH600 Coulter Analysis Systems because the optical degradation may potentially cause a delay in reporting results for nuc |
| 2013-11-08 | Beckman Coulter Inc. | Beckman Coulter is recalling the UniCel DxH800 and UniCel DxH600 Coulter Analysis Systems because the optical degradation may potentially cause a delay in reporting results for nuc |
Query this across every FDA database — by API.
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.