Home › Device types › LRR
First Aid Kit With Drug
FDA product code LRR · Class N · Unknown
3,390
Registered devices
25
Adverse events
30
Recalls
15
510(k) clearances
Devices with this code
CUSTOM — AERO HEALTHCARE (US), LLCFirst Aid Only — Acme United Corporation36M - Class B 21 Lawson - Metal — Certified Safety Manufacturing, Inc.First Aid Only — Acme United Corporation36M - State of Colorado DOT - Med Facility — Certified Safety Manufacturing, Inc.AEROKIT — AERO HEALTHCARE (US), LLCFirst Aid Only — Acme United CorporationFirst Aid Only — Acme United CorporationFirst Aid Only — Acme United Corporation10PW - Nevada Body Fluid — Certified Safety Manufacturing, Inc.FAC-4 - Miller & Long Concrete — Certified Safety Manufacturing, Inc.75V - UP Facilities — Certified Safety Manufacturing, Inc.Class A 21 Assortment Pack — Certified Safety Manufacturing, Inc.First Aid Only — Acme United CorporationFirst Aid Only — Acme United CorporationSafety General Purpose — Certified Safety Manufacturing, Inc.Bloodborne Pathogen Cabinet Refill - 100 Piece — ULINE, INC.OP - First aid series — Yiwu Ori-Power Medtech Co.,Ltd.First Aid Only — Acme United CorporationFirst Aid Only — Acme United CorporationFirst Aid Only — Acme United CorporationNew Hampshire BFK - 10 Refill — Certified Safety Manufacturing, Inc.First Aid Only — Acme United CorporationAdventure Medical Kits — Adventure Ready Brands
Recent 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 E |
| 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 tablet |
| 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 tablet |
| 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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.