FDA Device recall Z-1945-2020
iQ200 Series Urine Microscopy Analyzer- All part numbers
- FDA Device
- Class II
- terminated
- Published 2020-05-20
On 2020-05-20 the FDA classified a Class II recall of iQ200 Series Urine Microscopy Analyzer- All part numbers by Beckman Coulter, citing A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or m….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1945-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-03-30 |
| Published | 2020-05-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Beckman Coulter |
| Distribution | US |
Product
iQ200 Series Urine Microscopy Analyzer- All part numbers
Reason
A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or melting of the SATA adapter cable within the computer s metal enclosure, smoke emanating from PC6, flames contained within PC6, or an inability to use the device s CD-ROM.
Identifiers
| code_info | Catalog Numbers: 00-3322, 700-3325, 700-3326, 700-3345, 700-3347, 700-3370, 700-3375, 700-3300RFB, B48999, C10683, C10684., All part numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1945-2020%22
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