AutoMate 1200 Catalog Number ODL25120 — Class II medical device recall Z-1169-2018
Completed recall by Beckman Coulter Inc., reported 2018-03-28. Belts on the x-axis (and on the y-axis, to a lesser extent) manufactured from 2015 are showing premature failu
| Recall number | Z-1169-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2018-01-19 |
| Classified | 2018-03-22 |
| Reported by FDA | 2018-03-28 |
| Countries outside the US | AT, AU, BE, BR, CA, CH, CN, CY, CZ, DE, DK, ES, FI, FR, GB, GR, HK, HR, HU, IE, IL, IN, IT, KR, KW, LT, LV, MX, NL, NO, NZ, PA, PL, PT, QA, RU, SA, SE, SG, SI, SK, TR, TW, ZA |
| Quantity | 98 units |
| Serial numbers | ODL25120 |
| Model numbers | ODL25120, ODL25125, ODL25250, ODL25255 |
Product
AutoMate 1200 Catalog Number ODL25120; AutoMate 1250 Catalog Number ODL25125; AutoMate 2500 Catalog Number ODL25250; AutoMate 2550 Catalog Number ODL25255
Reason for recall
Belts on the x-axis (and on the y-axis, to a lesser extent) manufactured from 2015 are showing premature failure, posing the remote risk of cross-contamination.
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-1169-2018. 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.