Enzymatic Creatinine Reagent — Class II medical device recall Z-2080-2017
Terminated recall by Beckman Coulter Inc., reported 2017-05-24, distributed in PR. Beckman Coulter has identified the following drugs as potential sources of interference: Metamizole (Dipyrone)
| Recall number | Z-2080-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beckman Coulter Inc., Brea, CA, United States |
| Recall initiated | 2017-04-03 |
| Classified | 2017-05-12 |
| Reported by FDA | 2017-05-24 |
| Terminated | 2018-05-31 |
| Distributed | PR |
| Countries outside the US | AE, AU, BD, BE, BG, CA, CH, CN, CO, CZ, DE, EG, ES, FI, FR, GB, GH, GR, GT, HK, IE, IN, IT, JO, JP, KR, KW, LB, LT, MX, MY, NL, NZ, OM, PA, PH, PK, PL, PT, PY, QA, RO, RS, RU, SA, SE, SG, SK, TH, TR, TW, VN, ZA |
| Model numbers | A60298 |
Product
Enzymatic Creatinine Reagent (CR-E 2 x 200), Catalog No. A60298. Intended for the quantitative determination of creatinine (CR-E) concentration in human serum, plasma or urine.
Reason for recall
Beckman Coulter has identified the following drugs as potential sources of interference: Metamizole (Dipyrone), Sulfasalazine, and Sulfapyridine and may result in false low results.
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-2080-2017. 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.