iQ200 Series Urine Microscopy Analyzer- All part numbers — Class II medical device recall Z-1945-2020
Terminated recall by Beckman Coulter Inc., reported 2020-05-20, distributed nationwide. A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electr
| Recall number | Z-1945-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2020-03-30 |
| Classified | 2020-05-08 |
| Reported by FDA | 2020-05-20 |
| Terminated | 2023-08-31 |
| Distributed | Nationwide (US) |
| Quantity | 3,576 units |
| Model numbers | 00-3322, 700-3300RFB, 700-3325, 700-3326, 700-3345, 700-3347, 700-3370, 700-3375, B48999, C10683, C10684, IQ200 |
Product
iQ200 Series Urine Microscopy Analyzer- All part numbers
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1945-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.