Microbiologics recalls KWIK-STIK QC Sets and Panels due to potential contamination with E. coli, Staphylococcus epidermidis, and S. warneri. Affected units have specific lot numbers and expiration dates.
Potential contamination with Escherichia coli Staphylococcus epidermidis and S. warneri.
Microbiologics is recalling its KWIK-STIK QC Sets and Panels because they may be contaminated with harmful bacteria including E. coli, Staphylococcus epidermidis, and S. warneri. This could pose a health risk if the products are used in laboratory settings without proper sterilization.
The products may contain harmful bacteria such as E. coli, Staphylococcus epidermidis, and S. warneri. If these contaminated products are used in laboratory settings without proper sterilization, they could pose a health risk.
Laboratory users who own or use the KWIK-STIK QC Sets and Panels are most at risk. The recall affects specific lot numbers and expiration dates.
Check for lot numbers 5193-10 (expires 09/30/2021) or 5193-11 (expires 04/30/2021) on the packaging. The product is sold in packs of 2 with a unique identifier UDI: 70845357030718.
Look for lot numbers 5193-10 (expires 09/30/2021) or 5193-11 (expires 04/30/2021) on the packaging.
The products may contain harmful bacteria including E. coli, Staphylococcus epidermidis, and S. warneri.
Check for lot numbers 5193-10 (expires 09/30/2021) or 5193-11 (expires 04/30/2021) on the packaging. The product is sold in packs of 2 with a unique identifier UDI: 70845357030718.
The recall does not specify a remedy, so contact Microbiologics directly for guidance.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-0584-2022 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-0584-2022 from Microbiologics. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
