FDA Device recall Z-0308-2024
LYFO-DISK, P. venetum, Catalog number 0794L
- FDA Device
- Class II
- ongoing
- Published 2023-11-22
On 2023-11-22 the FDA classified a Class II recall of LYFO-DISK, P. venetum, Catalog number 0794L 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-0308-2024 |
| 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
LYFO-DISK, P. venetum, Catalog number 0794L
Reason
A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
Identifiers
| code_info | UDI/DI 10845357019186, Lot Numbers: 794-142-1 |
|---|
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-0308-2024%22
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