FDA Device recall Z-0504-2022
Gentueri Viral Transport Medium (VTM), Sterile, IVD
- FDA Device
- Class II
- terminated
- Published 2022-01-26
On 2022-01-26 the FDA classified a Class II recall of Gentueri Viral Transport Medium (VTM), Sterile, IVD by Gentueri, citing medium showed visual turbidity and discoloration, potentially contaminating samples transported for testing.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0504-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-03-18 |
| Published | 2022-01-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Gentueri |
| Distribution | US |
Product
Gentueri Viral Transport Medium (VTM), Sterile, IVD
Reason
Medium showed visual turbidity and discoloration, potentially contaminating samples transported for testing.
Identifiers
| code_info | CAT #: 3300-000; Lot #: 1142 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0504-2022%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.