FDA Device recall Z-0511-2022
KWIK-STIK 2 Pack, Catalog #0894P
- FDA Device
- Class II
- terminated
- Published 2022-01-26
On 2022-01-26 the FDA classified a Class II recall of KWIK-STIK 2 Pack, Catalog #0894P by Microbiologics, citing contamination with S. epidermidis.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0511-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-12-16 |
| Published | 2022-01-26 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microbiologics |
| Distribution | CA, IA, IL, LA, MA, MI, NY, PA, SD, TN, VA, WI, WV |
Product
KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.
Reason
Contamination with S. epidermidis
Identifiers
| code_info | KWIK-STIK 2 Pack - Catalog#: 0894P, Lot #: 894-68-3, Exp. 6/30/2022, 894-68-4, Exp. 6/30/2022, UDI: 20845357022947;…KWIK-STIK 2 Pack - Catalog#: 0894P, Lot #: 894-68-3, Exp. 6/30/2022, 894-68-4, Exp. 6/30/2022, UDI: 20845357022947; KWIK-STIK 6 Pack - Catalog#: 0894K, Lot #: 894-68-1, Exp. 6/30/2022, UDI: 30845357022951; LYFO DISK - Catalog#: 0894L, Lot #: 894-68-2, Exp. 6/30/2022, UDI: 10845357022964; |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0511-2022%22
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