FDA Device recall Z-3019-2018
remel THIOGLYCOLLATE MEDIUM, REF 05152
- FDA Device
- Class II
- terminated
- Published 2018-09-19
On 2018-09-19 the FDA classified a Class II recall of remel THIOGLYCOLLATE MEDIUM, REF 05152 by Remel, citing products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3019-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-08-13 |
| Published | 2018-09-19 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Remel |
| Distribution | n/a |
Product
remel THIOGLYCOLLATE MEDIUM, REF 05152
Reason
Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.
Identifiers
| code_info | Lot number: 258192 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Other recalls by Remel
- GC Agar Base (150mm) 10/PK R04030
FDA Device · Class II · 2026-07-08 · Remel - Yeastone Broth, 11ML, 10/BOX YY3462
FDA Device · Class II · 2026-04-22 · Remel - Campy CVA Medium 100/PK, R01272
FDA Device · Class II · 2026-03-04 · Remel - 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
FDA Device · Class II · 2025-12-03 · Remel - Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
FDA Device · Class II · 2025-08-06 · Remel
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3019-2018%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.