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Signature Care

BETTER LIVING BRANDS LLC · Model 321130195894 · UDI-DI 00321130195894

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

Description

First Aid Kit, First Aid Essentials, 70 items including 1 carrying case: 5 - Fabric Bandages 1 IN x 3 IN (25 mm x 76 mm); 10 - Fabric Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 15 - Fabric Bandages 5/8 IN x 2 1/4 IN (15 mm x 57 mm); 21 - Sheer Bandages 3/4 IN x 3 IN (19 mm x 76 mm); 4 - Triple Antibiotic Ointment 0.03 OZ (0.9 g); 6 - Hand Cleansing Wipes 4 3/4 IN x 7 3/4 IN (120 mm x 196 mm); 8 - Sterile Pads 2 IN x 2 IN (50 mm x 50 mm); 1 - Carrying Case

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.