Home › ULINE, INC. › BLEED CONTROL KIT
BLEED CONTROL KIT
ULINE, INC. · Model S-25331 · UDI-DI 10850015055482
0
510(k) clearances
5
Adverse events
1
Recalls
236
Facilities
Description
Windless Tourniquet Elastic Band Back-Up Tourniquet Hema-Seal Trauma Dressing Emergency Blanket Trauma Pad Nitrile Exam Gloves Bandage Shears to Cut Clothing Marker to Note Tourniquet Time Bleeding Control Product Use Guidelines Wall Mounting Kit
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2026-07-07 | INTEGRATED MEDCRAFT LLC | Devices could potentially contain an occluded or partially occluded Guedel Airway tip. |
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 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.
