bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated… — Class II medical device recall Z-2874-2018
Terminated recall by Biomerieux Inc, reported 2018-08-29, distributed nationwide. Missing desiccant.
| Recall number | Z-2874-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomerieux Inc, Hazelwood, MO, United States |
| Recall initiated | 2018-01-23 |
| Classified | 2018-08-17 |
| Reported by FDA | 2018-08-29 |
| Terminated | 2021-07-13 |
| Distributed | Nationwide (US) |
| Quantity | 57 cartons |
| Lot numbers | 245057043 |
| Expiration dates | 2019-06-19 |
Product
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent cards designed for the ID and antimicrobial susceptibility testing of bacteria and yeast.
Reason for recall
Missing desiccant.
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-2874-2018. 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.