FDA Device recall Z-0876-2026
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
- FDA Device
- Class II
- ongoing
- Published 2025-12-10
On 2025-12-10 the FDA classified a Class II recall of KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K by Microbiologics, citing some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0876-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-13 |
| Published | 2025-12-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Microbiologics |
| Distribution | n/a |
Product
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Reason
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
Identifiers
| code_info | UDI-DI: 30845357020018; Lot Number: 818-111-7 |
|---|
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-0876-2026%22
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