HF Acquisition Co LLC Brand Name: Sporetraq Mail-In Spore Testing Service recall: Due to incorrect incubation process being performed on product
Due to incorrect incubation process being performed on product.
The hazard: Harmful chemical exposure
This notice concerns a chemical found in the product at a level regulators consider unsafe, which is usually caught by laboratory testing rather than by anybody noticing a problem.
What the notice says: Due to incorrect incubation process being performed on product.
Why it matters: A chemical that should not be present at this level was found in the product. Depending on the substance, the concern may be a burn or irritation on contact, or a long-term risk from repeated exposure.
Symptoms and when to call a doctor
For a splash or spill, rinse the skin or eyes with running water for 15 to 20 minutes and remove contaminated clothing. If the product was swallowed, or if there is any trouble breathing, call Poison Control on 1-800-222-1222, which operates free and around the clock — or 911 if the person is collapsing, struggling to breathe or unconscious. Take the container or a photo of the label with you to any appointment.
This page is general information, not medical advice. If you feel unwell, a clinician who can see you is the only person able to judge your case.
Recall details
- Recall number
- Z-2332-2026
- Published
- June 17, 2026
- Risk level
- Class II
- Status
- Ongoing
- Issued by
- U.S. Food and Drug Administration
- Brand
- HF Acquisition Co LLC
- Product type
- Medical devices
- Units affected
- 0
- Distribution
- Nationwide
- Made in
- United States
- Lot / code info
- Lot Code: Please see attached spreadsheet listing products that were not incubated per the following requirements : a. Spore strips used in steam sterilizers are incubated for 24 hours b. Spore strips used in chemiclave sterilizers are incubated for 72 hours c. Spore strips used in dry heat or ethylene oxide sterilizers are incubated for 7 days As noted in the previous recall scope question, HealthFirst's Field Correction scope will be expanded to include notifications to all customers in possession of 1023780 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS,1023770 SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS or other products serviced by Mesa Labs.
Products covered by this recall
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS Model/Catalog Number: 1023770 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 12 bacterial Spore Strips provided by Mesa Labs. The Spore Strip (single species G. stearothermophilus ATCC#7953 or dual species G. stearothermophilus ATCC #7953 and B. atrophaeus ATCC #9372) is intended for use in testing the efficacy of sterilizer systems used in healthcare facilities. The Spore Strips are compatible with Steam sterilization, Chemiclave¿ sterilization, Ethylene Oxide sterilization, or Dry Heat sterilization processes. The test strip is placed in the customer s sterilizer during their sterilization cycle and upon completion the sterilized test strip along with the control strip is returned to Mesa Labs for lab testing in the return envelope. Spore test results are digitally stored in HealthFirst s OnTraq smart automation tracking and reporting system for easy and secure access to a paperless archive from any device with internet access. Component: N/A
Check your product
The notice names 1 code you can read straight off the package. Type the one printed on yours and the list below narrows to it.
Model or item number
On the rating label, the box or the instruction sheet.
- 1023770 Software Version
Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.
What to do about Chemical
HF Acquisition Co LLC — This notice concerns a chemical found in the product at a level regulators consider unsafe, which is usually caught by laboratory testing rather than by anybody noticing a problem.
- Stop using the product and keep it away from children and pets.
- Do not pour it down a drain or into a bin without checking local hazardous-waste rules, and never mix it with another cleaner.
- Ventilate the room if the product was sprayed or applied there.
- Keep the container — the lot code on it is what a refund claim and any medical follow-up both depend on.
How the remedy works
CPSC recalls specify one of three remedies, and which one you get is not negotiable — but how smoothly it goes often is.
- A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.
- Return shipping is the company’s cost. If you are asked to pay it, push back.
- A repair kit is shipped free and is designed to be fitted at home; if you cannot fit it, ask whether they will arrange installation.
- A replacement is usually the current model, not the recalled one. Confirm the replacement is not itself under recall.
Company contact: HF Acquisition Co LLC — 11629 49th Pl W, Mukilteo, WA, 98275-4255
The official notice
This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.
Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls
Questions people ask about this recall
Why was HF Acquisition Co LLC medical devices recalled?
Due to incorrect incubation process being performed on product. Due to incorrect incubation process being performed on product.
How do I know if I have the recalled product?
Match the codes printed on your package against the notice: model number 1023770 Software Version. If the code on your package is not on that list, your unit is outside the recall.
What should I do with it right now?
Stop using the product and keep it away from children and pets.
Can I get my money back?
A refund means the purchase price back, sometimes prorated by age for durable goods. Ask how they calculated it if the figure looks low.
Where was the recalled product sold?
It was distributed nationwide.
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