Home › HF ACQUISITION CO. LLC › MOBILE ACLS V2 EMERGENCY MEDICAL KIT
MOBILE ACLS V2 EMERGENCY MEDICAL KIT
HF ACQUISITION CO. LLC · Model 1003471 · UDI-DI 00850065007342
LRR
Prescription
10
510(k) clearances
12
Adverse events
30
Recalls
143
Facilities
Description
To prepare physicians and dental practices with advanced cardiac life support medications to respond to medical emergencies until EMS arrives.
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-03-27 | North American Rescue LLC. | Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5 Error Code where the |
| 2022-06-23 | Family Dollar Stores, Llc. | Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022. |
| 2022-04-05 | Certified Safety Mfg Inc | First aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer. |
| 2022-03-11 | Total Resources Intl | ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due |
| 2022-03-11 | Total Resources Intl | ULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due |
| 2022-03-02 | ASO LLC | Kits contained recalled acetaminophen. |
| 2020-06-05 | HF Acquisition Co. LLC | A missing component (hand suction pump) in the emergency medical kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
| 2020-06-04 | HF Acquisition Co., LLC | Instead of 2 doses, packaged 1 dose of nasal spray in an emergency kits. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.