Medical DeviceJun 17, 2026
SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS recall — FDA Z-2331-2026
Due to incorrect incubation process being performed on product.
Class IIFDA: OngoingHF Acquisition Co LLC
Recall history in this database
Classification mix: Class II: 8, Class III: 1.
Medical DeviceJun 17, 2026
SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 12 TESTS recall — FDA Z-2332-2026
Due to incorrect incubation process being performed on product.
Class IIFDA: OngoingHF Acquisition Co LLC
Medical DeviceFeb 19, 2025
HF Acquisition Co Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item recall — FDA Z-1141-2025
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…
Class IIFDA: OngoingHF Acquisition Co LLC
Medical DeviceAug 19, 2020
HF Acquisition Co STAT KIT Model 550AI Emergency Medical Kit recall — FDA Z-2791-2020
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Class IIFDA: TerminatedHF Acquisition Co., LLC
Medical DeviceAug 19, 2020
HF Acquisition Co STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various recall — FDA Z-2790-2020
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Class IIFDA: TerminatedHF Acquisition Co., LLC
Medical DeviceAug 19, 2020
HF Acquisition Co STAT KIT, Model SM30 recall — FDA Z-2789-2020
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Class IIFDA: TerminatedHF Acquisition Co., LLC
Medical DeviceAug 19, 2020
HF Acquisition Co STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is recall — FDA Z-2779-2020
A missing component (hand suction pump) in the emergency medical kits.
Class IIFDA: TerminatedHF Acquisition Co. LLC
Medical DeviceAug 19, 2020
HF Acquisition Co HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150 recall — FDA Z-2788-2020
Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Class IIFDA: TerminatedHF Acquisition Co., LLC
DrugJul 29, 2020
Famotidine Injection, USP, 20 mg/2mL, 2 mL vial recall — FDA D-1392-2020
TEMPERATURE ABUSE: Complaint received from customer that product was received in a non-refrigerated state.
Class IIIFDA: TerminatedHF Acquisition Co. LLC
Understanding this recall history
This page summarizes recall records in which the official source identifies HF Acquisition Co., LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.