Reported Mar 9, 2022 · Terminated
KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from…
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 asKWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299
- Lot codes and dates
- Catalog Number HL163263 OEM Private Label with Healthlink
- UDIN/A (OEM agreement with Healthlink ended in Q1 2016 before UDI was required for class 1
- IVDs) Lot Number (Expiration Date)
959-74-1 (10/08/2014)959-75-2 (04/22/2015)959-75-3 (04/22/2015)959-75-6 (04/22/2015)959-75-7 (04/22/2015)959-75-10 (04/22/2015)and 959-76-2 (07/08/2015)
- Amount recalled
- 150 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
- PR
Why it was recalled
This strain should be resistant to high levels of Gentamicin and be resistant to Gentamicin Synergy. A specific lot was found susceptible to Gentamicin Synergy during in-house testing.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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