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Uline 25 Person First Aid Kit - SUB

ULINE, INC. · Model H-1293-S1 · UDI-DI 10850015055307

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510(k) clearances

Adverse events

Recalls

146

Facilities

Description

"(1) ABSORBENT COMPRESS (10) ANTIBIOTIC OINTMENT (10) ANTISEPTIC TOWELETTE (6) BURN CREAM (1) CPROTECTOR (1) EYE PAD (16) FABRIC BANDAGE (5) FABRIC FINGERTIP BANDAGE (4) FABRIC KNUCKLE BANDAGE (1) FIRST AID FACTS GUIDE (1) FIRST AID TAPE (1) PLASTIC TWEEZERS (4) GAUZE PAD (1) GAUZE ROLL (1) INSTANT ICE PACK (2) NITRILE GLOVE (16) PLASTIC BANDAGE (1) SCISSORS (1) SINGLE USE SALINE (1) TRIANGULAR BANDAGE"

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.