FDA Device recall Z-0209-2018
CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres
- FDA Device
- Class II
- terminated
- Published 2017-12-13
On 2017-12-13 the FDA classified a Class II recall of CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres by Remel, citing product may have incorrect cation information detailed on the product label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0209-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-11-02 |
| Published | 2017-12-13 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Remel |
| Distribution | AL, MD, ME, NC, TN |
Product
CM0405 Mueller-Hinton Broth IVD, 500g makes 23.8 litres.
Reason
Product may have incorrect cation information detailed on the product label.
Identifiers
| code_info | Lot 1865331, Exp. 06/2021 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0209-2018%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.