HF Acquisition Co LLC recalls SPORETRAQ Mail-In Spore Testing Service (12 tests) due to incorrect incubation process. Affected units may not test sterilizer efficacy properly.
Due to incorrect incubation process being performed on product.
HF Acquisition Co LLC is recalling SPORETRAQ Mail-In Spore Testing Service (12 tests) because the incubation process was performed incorrectly. This could lead to inaccurate sterilizer effectiveness testing, which is critical for healthcare facilities using sterilization systems.
The SporeTraq test strips require specific incubation times based on the sterilization method (24 hours for steam, 72 hours for chemiclave, 7 days for dry heat or ethylene oxide). Incorrect incubation leads to inaccurate results, which could mean sterilizers aren't working properly.
Healthcare facilities that use SPORETRAQ Mail-In Spore Testing Service for sterilizer validation. Facilities using the 12-test version (model 1023770) are most at risk.
Check for the model number 1023770 on the SPORETRAQ Mail-In Spore Testing Service (12 tests) product. This was sold to healthcare facilities for sterilizer validation testing.
Verify if the incubation time matches the sterilizer type: 24 hours for steam, 72 hours for chemiclave, 7 days for dry heat or ethylene oxide.
The recall is due to incorrect incubation process being performed on the product, which can lead to inaccurate sterilizer effectiveness testing.
The model number is 1023770 for the SPORETRAQ Mail-In Spore Testing Service (12 tests).
Healthcare facilities using this product may get inaccurate results, meaning they might not know if their sterilizers are working properly.
We’ve drafted a message you can send SPORETRAQ to request your refund or repair — edit it as you like.
Subject: Recall Z-2332-2026 — SPORETRAQ SPORETRAQ Hello, I own a SPORETRAQ that is covered by recall Z-2332-2026 from SPORETRAQ. 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.
