FDA Device recall Z-0307-2024
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
- FDA Device
- Class II
- ongoing
- Published 2023-11-22
On 2023-11-22 the FDA classified a Class II recall of KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack) by Microbiologics, citing A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0307-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-10-18 |
| Published | 2023-11-22 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microbiologics |
| Distribution | US |
Product
KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
Reason
A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
Identifiers
| code_info | a) UDI/DI 20845357019169, Lot Numbers: 794-142-2, 794-142-4 b) UDI/DI 30845357019173, Lot Numbers: 794-142-3 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0307-2024%22
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