Microbiologics KWIK-STIK Plus Recall: Labeling Error Hazard
Microbiologics recalls KWIK-STIK Plus products with labeling error. Affected items have specific catalog, lot, and expiration numbers. No action needed per recall details.
Lower-risk recall
Labeling error.
Contact the company
What happened, in plain English
Microbiologics is recalling KWIK-STIK Plus products due to a labeling error. This issue does not pose a safety risk to users and requires no action. Read more at govinfonow.com/recall/60722-microbiologics-kwik-stik-plus-recall-labeling-error-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/60722-microbiologics-kwik-stik-plus-recall-labeling-error-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1125-2022
Cite this page
“Microbiologics KWIK-STIK Plus Recall: Labeling Error Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60722-microbiologics-kwik-stik-plus-recall-labeling-error-hazard. Based on FDA recall #Z-1125-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1125-2022%22&limit=1).
Why it’s dangerous
The labeling error means the product's identification details are incorrect. This could lead to confusion about the product's specifications but does not cause physical harm or injury.
Who’s affected
Users of KWIK-STIK Plus products with catalog number 0801P, lot number 801-44-4, and expiration date 05/31/2023 are affected. No one is at risk from this labeling error.
How to tell if you have this one
Check for catalog number 0801P, lot number 801-44-4, and expiration date 05/31/2023 on the product packaging. This labeling error does not affect product safety.
- Brand
Microbiologics- Category
Medical device
What to do — step by step
Check Product Details
Verify the catalog number, lot number, and expiration date on the product packaging to confirm if it is affected.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 2 states.
FDA distribution: “Distributed US Nationwide to IA, TN and internationally to Mexico, Colombia, France, South Africa, United Kingdom.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Iowa, Tennessee.
Recall timeline
FDA terminated this recall 20 months after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1125-2022 (May 6, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1125-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 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.