Reported Feb 16, 2022 · Terminated
KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC…
Microbiologics Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Microbiologics Inc · 200 Cooper Ave N · Saint Cloud, MN · 56303-4440
Is this the product you have?
- KWIK-STIK, Quality control kit for culture media
- sold asa. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299
- Lot codes and dates
- a. Catalog Number 0959P
- UDI20845357023210
- Lot Number (Expiration Date)
959-94-3 (04/30/2020)959-95-2 (09/30/2020)959-96-1 (12/31/2020)959-96-4 (12/31/2021)959-97-4 (03/31/2021)959-97-5 (03/31/2021)b. Catalog Number 0959K
- UDI30845357023224
- Lot Number (Expiration Date)
959-94-2 (04/30/2020)959-95-1 (09/30/2020)959-95-5 (09/30/2020)959-96-3 (12/31/2020)959-97-1 (03/31/2021)959-97-6 (03/31/2021)
- Amount recalled
- 1,975 units
This recall covers 11 products
The agency filed one notice per product. You are reading one of them; the other 10 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
Tests returning incorrect susceptible results. High Level Gentamicin Synergy value was out of specification (sensitive) when analyzed on the Vitek 2 AST-GP67 card, and these lots failed the disk diffusion method used for product release.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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