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WOUND CARE TREATMENT PACK
ULINE, INC. · Model S-25619 · UDI-DI 10850015055628
10
510(k) clearances
25
Adverse events
30
Recalls
146
Facilities
Description
3X3" STERILE GAUZE PAD (2 PACK) HAND SANITIZER 0.9GM BULK NITRILE EXAM GLOVES 2/BAG BZK WIPES, FAO, 5X7 SINGLE WIPE ALCOHOL PREP PAD, FAO, SOLDIER, STERILE NEOMMYCIN ANTIBIOTIC OINTMENT 0.9G BULK BANDAGE PLASTIC 1X3" 5-UP 1X3" FABRIC ADHESIVE BANDAGES 5-UP 2"X4YD NS GAUZE ROLL BULK 5"X9" COMBINE DRESSING BULK EMERGENCY BLANKET
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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Get your free API keyRead the docsData 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.