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Detergent

FDA product code JCB · Class 1 · Pathology

107
Registered devices
32
Adverse events
3
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-08-29Microcare MedicalContaminated equipment and packaging caused Klebsiella oxytoca, Enterobacter asburiae, Enterobacter bugandensis, pathogenic and opportunistic bacteria, to occur
2013-11-08Beckman 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 repor
2013-11-08Beckman 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 repor

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.