Microbiologics recalls KWIK-STIK 2-Pack products that may fail to recover Campylobacter jejuni subsp. jejuni. Affected units have Catalog Number 0325P and specific lot numbers. No remedy is stated.
“Microbiologics KWIK-STIK 2-Pack: Microorganism Recovery Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/50554-microbiologics-kwik-stik-2-pack-microorganism-recovery-risk. Based on FDA recall #Z-0984-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0984-2026%22&limit=1).
The FDA announced on Dec. 2, 2025, that Microbiologics Inc is recalling KWIK-STIK 2-Pack products due to a potential failure to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428. The agency issued recall number Z-0984-2026 for the voluntary Class II action.
Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428, according to the FDA.
Context
GovInfoNow's records show Microbiologics Inc has 35 other recalls on record since June 6, 2017. Other recent recalls of similar products include Microbiologics KWIK-STIK Quality Control Kit Recall (Nov. 13, 2025), Microbiologics LYFO-DISK Recall (June 27, 2025), and Microbiologics KWIK-STIK and LYFO DISK recall (June 17, 2025). Other recent recalls of similar products include Remel Campy CVA Medium 100/PK recall (Feb. 5, 2026), GET TESTED Gut Microbiome Test Large (Nov. 3, 2025), and Medline Neuro Pack Kits Contaminated with Bacillus Species - Recall (June 11, 2026).
How to tell if you have this one
Check for Catalog Number 0325P on the product label. Affected units have specific lot numbers: 325-120-3, 325-120-7, and additional lots added on 12/22/25: 325-119-1, 325-119-5.
Brand
Microbiologics
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
Worldwide - US Nationwide.
Recall number
Product, codes & lots
Quantity
Z-0984-2026
KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P; UDI-DI: 20845357006459; Lot Numbers: 325-120-3, 325-120-7, Additional Lots added 12/22/25: 325-119-1, 325-119-5
86 units (127 additional units 12/22/25)
Z-0985-2026
KWIK-STIK 6-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325K; UDI-DI: 30845357006463; Lot Numbers: 325-120-1, 325-120-4, 325-120-6, Additional Lots added 12/22/25: 325-119-2
18 units (9 additional units 12/22/25)
Z-0986-2026
LYFO DISK, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325L; UDI-DI: 10845357006476; Lot Numbers: 325-120-5, Additional lots added 12/22/25: 325-119-3, 325-119-6
1 unit (16 additional units added 12/22/25)
Based on the official FDA remedy
What to do — step by step
Check Product Details
Identify if your KWIK-STIK 2-Pack has Catalog Number 0325P and the listed lot numbers.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA distribution: “Worldwide - US Nationwide.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA published this recall 29 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0984-2026 (December 2, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0984-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.