HF Acquisition Co. LLC
4 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (4)
Devices registered here (1)
- First Aid Kit With DrugProduct code LRR (opens in a new tab) · Not classified · Unknown
Recalls & enforcement
- Class IIOngoing2026-04-13Due to incorrect incubation process being performed on product.
- Class IIOngoing2024-12-11Spore 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.
- Class IITerminated2020-06-05A missing component (hand suction pump) in the emergency medical kits.
- Class IITerminated2020-06-04Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “HF Acquisition Co. LLC (FEI 3014534) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014534-hf-acquisition-co-llc/
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