FDA Device recall Z-2124-2025
KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L
- FDA Device
- Class II
- ongoing
- Published 2025-07-23
On 2025-07-23 the FDA classified a Class II recall of KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L by Microbiologics, citing affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for th….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2124-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-06-17 |
| Published | 2025-07-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Microbiologics |
| Distribution | OH, UT |
Product
KWIK-STIK and LYFO DISK, quality control kit for culture media Catalog # 0805K and 0805L
Reason
Affected products contain Staphylococcus epidermidis instead of the expected Brevundimonas diminuta. This may cause the user's quality control to fail and delayed diagnosis for the patient.
Identifiers
| code_info | Lot #: 805-234-4, 805-234-5 UDI: (0805K) 30845357019531, (0805L) 10845357019544 |
|---|
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-2124-2025%22
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