MRSASelect II — Class II medical device recall Z-1743-2019
Terminated recall by Bio-Rad Laboratories, Inc, reported 2019-06-12, distributed nationwide. Abnormal coloration of agar plates and the growth of non-characteristic MRSA colonies.
| Recall number | Z-1743-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bio-Rad Laboratories, Inc, Redmond, WA, United States |
| Recall initiated | 2018-06-08 |
| Classified | 2019-06-06 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-10-30 |
| Distributed | Nationwide (US) |
| Quantity | 3,632 units |
| Lot numbers | 64177778, 64179165, 64182547, 64184389, 64187554, 64189124, 64190805 |
| Model numbers | 63758 |
| Expiration dates | 2018-06-10, 2018-06-17, 2018-07-03, 2018-07-08, 2018-07-22, 2018-07-23, 2018-07-31 |
Product
MRSASelect II, IVD, REF 63758 (20 plates per package). The MRSASelect is indicated for use in conjunction with other laboratory tests and clinical data available to aid in the identification and diagnosis of MRSA from patients with skin and soft-tissue infections.
Reason for recall
Abnormal coloration of agar plates and the growth of non-characteristic MRSA colonies.
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-1743-2019. 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.