Manufacturer

HF Acquisition Co., LLC

10 recalls in our database name HF Acquisition Co., LLC as the manufacturing or recalling firm.

What the numbers show

Total: 10
Critical: 0
Severe: 0
Most recent: 2026-06-17

Of the 10 recalls from HF Acquisition Co., LLC we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

Which agencies issued them

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–10 of 10

ModerateFDA (Devices)·Z-2332-2026·2026-06-17
SporeTraq 12-test mail-in spore testing service used incorrect incubation
The SporeTraq Mail-In Spore Testing Service, 12 tests, is being recalled because an incorrect incubation process was performed on the product.
Product
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 Strip
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2331-2026·2026-06-17
SporeTraq 52-test mail-in spore testing service used incorrect incubation
The SporeTraq Mail-In Spore Testing Service, 52 tests, is being recalled because an incorrect incubation process was performed on the product. 2,210 units are affected.
Product
Brand Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Product Name: SPORETRAQ MAIL-IN SPORE TESTING SERVICE, 52 TESTS Model/Catalog Number: 1023780 Software Version: N/A Product Description: The SporeTraq Mail-In Spore Testing Service includes 52 bacterial Spore Strip
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1141-2025·2025-02-19
Spore Test Monitoring System Printing Error May Cause Result Misdirection
HF Acquisition Co LLC is recalling Bio52 and Bio12 HealthFirst Mail In Monitoring Systems (4,021 units) due to a printing error on return envelopes that may cause spore test results to be reported to incorrect customer accounts.
Product
Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In Monitoring System, 12 Tests, Item: 1003580
Category
Medical Device
Distribution
50 states
ModerateFDA (Drugs)·D-0870-2023·2023-06-14
Glycopyrrolate Injection Vials Recalled Due to Labeling Mix-up
HF Acquisition Co LLC is recalling Glycopyrrolate Injection 0.2mg/mL due to a label mix-up affecting specific lots distributed in Texas, Arizona, and California.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
3 states
ModerateFDA (Devices)·Z-2779-2020·2020-08-19
HealthFirst STAT KIT Z-1000 Emergency Medical Kits Recalled for Missing Component
HF Acquisition Co. LLC is recalling two STAT KIT Z-1000 emergency medical kits because they are missing a hand suction pump component.
Product
STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2790-2020·2020-08-19
HF Acquisition Recalls STAT KIT 550 Emergency Medical Kits
HF Acquisition Co., LLC is recalling 155 STAT KIT Model 550 Emergency Medical Kits because they contain one dose of Narcan Nasal spray instead of two.
Product
STAT KIT Model 550 Emergency Medical Kit P/N: 1009580 containing various products to include Narcan Nasal spray, item number 1010300
Category
Medical Device
Distribution
39 states
ModerateFDA (Devices)·Z-2789-2020·2020-08-19
HF Acquisition Recalls Emergency Medical Kits with Missing Narcan Dose
HF Acquisition Co., LLC is recalling 95 STAT KIT Model SM30 emergency medical kits because they contain one dose of Narcan Nasal spray instead of two.
Product
STAT KIT, Model SM30 ; Emergency Medical Kit P/N: 1008670 containing various products to include Narcan Nasal spray, item number 1010300
Category
Medical Device
Distribution
39 states
ModerateFDA (Devices)·Z-2788-2020·2020-08-19
HealthFirst Emergency Medical Kit Recalled for Missing Narcan Dose
HF Acquisition Co. is recalling HealthFirst Emergency Medical Kits because they contain one dose of Narcan nasal spray instead of two.
Product
HealthFirst Emergency Medical Kit, Model SM 7, P/N: 1008150; Manufactured by HF Acquisition Co. LLC, 11629 49th Place West/Mukilteo, WA 98275, HealthFirst.com; Store at Room Temperature. 9036-2v.5 08/2017 containing various products to include Narcan Nasal spray, item number 1010
Category
Medical Device
Distribution
39 states
ModerateFDA (Devices)·Z-2791-2020·2020-08-19
HF Acquisition Recalls STAT KIT Emergency Medical Kits with Missing Narcan Dose
HF Acquisition Co., LLC is recalling STAT KIT Model 550AI Emergency Medical Kits because they contain one dose of Narcan Nasal spray instead of two.
Product
STAT KIT Model 550AI Emergency Medical Kit. P/N: 1010830 containing various products to include Narcan Nasal spray, item number 1010300
Category
Medical Device
Distribution
39 states
LowFDA (Drugs)·D-1392-2020·2020-07-29
HF Acquisition Recalls Famotidine Injection Due to Temperature Abuse
HF Acquisition Co. LLC is recalling specific lots of Famotidine Injection because a customer reported the product was received in a non-refrigerated state.
Product
FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
Category
Drug
Distribution
1 state