Microbiologics recalls KWIK-STIK 2 Pack (Catalog# 0778P, lot 778-65-3) that may contain Candida instead of Trichosporon dermatis. Consumers should contact the company for details.
KWIKSTIK 2 Pack (REF 0778P) and QC Set and Panels: KWIKSTIK YST Comprehensive QC Set (REF 5195P) contain product labeled as Trichosporon dermatis (T. dermatis) which may contain Candida Utilis instead of T. dermatis.
Microbiologics is recalling KWIK-STIK 2 Pack products that may contain Candida instead of Trichosporon dermatis. This could cause incorrect results in lab tests if used for medical purposes.
The product may contain Candida instead of Trichosporon dermatis, which could lead to incorrect lab test results. This might affect medical diagnoses if used for critical testing.
People who own KWIK-STIK 2 Pack (Catalog# 0778P, lot 778-65-3) or QC Sets for lab testing. Lab technicians using these products for medical testing are most at risk.
Check for Catalog Number 0778P and Lot Number 778-65-3 on the product packaging. The product is labeled as Trichosporon dermatis derived from ATCC 204094.
Reach out to Microbiologics for specific instructions on how to handle the recalled product.
The product may contain Candida instead of Trichosporon dermatis, which could cause incorrect lab test results. However, it is not considered a safety hazard for normal use.
Contact Microbiologics for specific instructions on how to handle the recalled product.
Check for Catalog Number 0778P and Lot Number 778-65-3 on the product packaging.
We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.
Subject: Recall Z-1690-2020 — Microbiologics Microbiologics Hello, I own a Microbiologics that is covered by recall Z-1690-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
