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ULINE CONTRACTOR FIRST AID KIT

ULINE, INC. · Model H-11036 · UDI-DI 10850015055581

LRR

510(k) clearances

Adverse events

Recalls

146

Facilities

Description

ANTIBIOTIC OINTMENT ANTISEPTIC TOWELETTE BURN DRESSING CPR MASK ELECTOLYTE DRINK MIX EMERGENCY RESCUE BLANKET EYE PAD FABRIC FINGERTIP BANDAGE FABRIC KNUCKLE BANDAGE FIRST AID / BURN CREAM FIRST AID GUIDE FIRST AID TAPE GAUZE PAD GAUZE ROLL HAND SANITIZER INSTANT ICE PACK NITRILE GLOVES PLASTIC BANDAGE SCISSORS SINGLE USE EYEWASH STING WIPES SUNSCREEN PACKETS TRAUMA PAD TRIANGULAR BANDAGE TWEEZERS

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.

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Data 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.