FDA Device recall Z-2195-2025
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L
- FDA Device
- Class II
- ongoing
- Published 2025-08-06
On 2025-08-06 the FDA classified a Class II recall of LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L by Microbiologics, citing KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2195-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-27 |
| Published | 2025-08-06 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Microbiologics |
| Distribution | US |
Product
LYFO-DISK, M. Canis Derived from ATCC 36299, packaged as: 1) REF 0894L
Reason
KWIK-STIK REF numbers: 0894P, 0894K and LYFO DISK" 0894L may result in failure to recover the target microorganism. All lots of REF 894-76 are impacted.
Identifiers
| code_info | 1) 0894L: UDI/DI 10845357021967, Lot Numbers 894-76-4 and 894-76-6 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2195-2025%22
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