CM0405 Mueller-Hinton Broth IVD — Class II medical device recall Z-0209-2018
Terminated recall by Remel Inc, reported 2017-12-13, distributed in AL, MD, ME, NC, TN. Product may have incorrect cation information detailed on the product label.
| Recall number | Z-0209-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2017-11-02 |
| Classified | 2017-12-07 |
| Reported by FDA | 2017-12-13 |
| Terminated | 2020-08-05 |
| Distributed | AL, MD, ME, NC, TN |
| Quantity | 7 units |
| Reason classes | labeling |
| Lot numbers | 1865331 |
| Expiration dates | 2021-06 |
Product
CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.
Reason for recall
Product may have incorrect cation information detailed on the product label.
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-0209-2018. 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.