PlainRecalls
FDA Devices Moderate Class II Ongoing

KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P

Reported: December 31, 2025 Initiated: December 2, 2025 #Z-0984-2026

Product Description

KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P

Reason for Recall

Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.

Details

Recalling Firm
Microbiologics Inc
Units Affected
86 units (127 additional units 12/22/25)
Distribution
Worldwide - US Nationwide.
Location
Saint Cloud, MN

Frequently Asked Questions

What product was recalled?
KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P. Recalled by Microbiologics Inc. Units affected: 86 units (127 additional units 12/22/25).
Why was this product recalled?
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 31, 2025. Severity: Moderate. Recall number: Z-0984-2026.