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Kroger

KROGER CO., THE · Model 041260369728 · UDI-DI 00041260369728

LRR

510(k) clearances

Adverse events

Recalls

143

Facilities

Description

First Aid Kit, All-Purpose First Aid Essentials, 70 items: 1 - Carrying Case, 4 - Triple Antibiotic Ointment 1/32 OZ (0.9 g); 8 - Gauze Pads 2 IN x 2 IN (50 mm x 50 mm); 5 - Antibacterial Fabric Bandages 1 IN x 3 IN (25 mm x 76 mm); 10 - Antibacterial Fabric Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 15 - Antibacterial Fabric Bandages 5/8 IN x 2 1/4 IN (15 mm x 57 mm); 21 - Antibacterial Sheer Bandages 1 IN x 3 IN (25 mm x 76 mm); 6 - Hand Cleansing Wipes 4 3/4 IN x 7 3/4 IN (120 mm x 196 mm)

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.