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Uline First Aid Kit - 50 Person

ULINE, INC. · Model H-1294 · UDI-DI 10851253007615

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

Description

ABSORBENT COMPRESS, ALCOHOL PREP PAD, ANTIBIOTIC OINTMENT, ANTISEPTIC TOWELETTE, ASPIRIN (2/PACKAGE), BURN CREAM, CPR MASK, ELASTIC BANDAGE, 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, NON-STICK PADS, PLASTIC BANDAGE, SCISSORS, SINGLE USE SALINE, STING WIPES, 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.