HF Acquisition recalls HealthFirst Mail-In Monitoring Systems with possible spore test errors causing incorrect customer account reporting. Affected units include 52-test and 12-test systems with specific serial numbers.
Spore test strip monitoring system, designed for routine monitoring of sterilization processes, may have a printing error on the return envelope that may cause spore test results to be reported to the incorrect customer's account.
HF Acquisition is recalling their HealthFirst Mail-In Monitoring Systems due to a potential printing error on return envelopes that could misreport spore test results to the wrong customer. This could lead to incorrect sterilization process monitoring and potential safety issues for users.
The system may have a printing error on the return envelope that causes spore test results to be reported to the wrong customer's account. This could lead to incorrect sterilization monitoring, potentially affecting the safety of the sterilization process.
Users of the HealthFirst Mail-In Monitoring Systems for sterilization process monitoring are affected. Those who have the 52-test or 12-test systems with specific serial numbers listed in the recall are most at risk.
Check for the HealthFirst Mail-In Monitoring System with 52 tests (Item: 1003600) or 12 tests (Item: 1003580). Look for specific serial numbers listed in the recall notice.
Verify if your system has the specific serial numbers listed in the recall notice for the 52-test or 12-test models.
The recall is due to a potential printing error on the return envelope that may cause spore test results to be reported to the wrong customer's account.
The 52-test model (Item: 1003600) and 12-test model (Item: 1003580) with specific serial numbers listed in the recall notice.
No, the recall does not require stopping use. The issue is a potential reporting error, not a safety hazard.
We’ve drafted a message you can send HF Acquisition to request your refund or repair — edit it as you like.
Subject: Recall Z-1141-2025 — HF Acquisition HF Acquisition Hello, I own a HF Acquisition that is covered by recall Z-1141-2025 from HF Acquisition. 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.
