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Uline First Aid Kit - 25 Person

ULINE, INC. · Model H-1293 · UDI-DI 10851253007608

LRR
10
510(k) clearances
13
Adverse events
30
Recalls
146
Facilities

Description

ABSORBENT COMPRESS, ANTIBIOTIC OINTMENT, ANTISEPTIC TOWELETTE, ASPIRIN (2/PACKAGE), BURN CREAM, CPR MASK, EYE PAD, FABRIC BANDAGE, FABRIC FINGERTIP BANDAGE, FABRIC KNUCKLE BANDAGE, FIRST AID FACTS GUIDE, FIRST AID TAPE, PLASTIC TWEEZERS, GAUZE PAD, GAUZE ROLL, INSTANT ICE PACK, NITRILE GLOVE, PLASTIC BANDAGE, SCISSORS, SINGLE USE SALINE, TRIANGULAR BANDAGE

Recalls

DateFirmReason
2026-03-27North 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
2022-06-23Family Dollar Stores, Llc.Affected product was not appropriately stored in temperature-controlled areas between April 30, 2022 - June 10, 2022.
2022-04-05Certified Safety Mfg IncFirst aid kit and cabinet components are being recalled by the supplier due to cGMP deviations at the manufacturer.
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-11Total Resources IntlULTRAtab Laboratories recalled Acetaminophen and electrolyte tablets that were later placed into Total Resources Intl kits. Acetaminophen and electrolyte tablets were recalled due
2022-03-02ASO LLCKits contained recalled acetaminophen.
2020-06-05HF Acquisition Co. LLCA missing component (hand suction pump) in the emergency medical kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead of 2 doses, packaged 1 dose of nasal spray in an emergency kits.
2020-06-04HF Acquisition Co., LLCInstead 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.