Ultrasonic Transducer Kits For use with the Access Family of… — Class II medical device recall Z-1737-2014
Terminated recall by Beckman Coulter Inc., reported 2014-06-18, distributed nationwide. Beckman Coulter is initiating a field action because some Ultrasonic Transducer Kits were potentially assemble
| Recall number | Z-1737-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2014-05-14 |
| Classified | 2014-06-09 |
| Reported by FDA | 2014-06-18 |
| Terminated | 2014-12-25 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, CH, CN, ES, FR, HK, IT, JP, MX, PT, TR, TW |
| Quantity | 82 units |
| Model numbers | 81600N, 973100, A25640, A30260, A71456, A71460 |
Product
Ultrasonic Transducer Kits For use with the Access Family of Immunoassay Systems*. *The Access Family of Immunoassay Systems includes the Access 2, UniCel DxI 800 and UniCel DxI 600, UniCel DxC 600i, and the UniCel DxC 880i, UniCel DxC 860i, UniCel DxC 680i, and UniCel DxC 660i systems.
Reason for recall
Beckman Coulter is initiating a field action because some Ultrasonic Transducer Kits were potentially assembled with incorrect mounting screws.
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-1737-2014. 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.