ASP Global, LLC.

Frequent Recalls
64
Recalls
0
Units Recalled
0
Injuries
0
Deaths

Categories: Medical Device

2026-10-07 to 2026-10-07

DateSourceProductBrandSeverityUnits
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable BB Tournquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable BB Tournquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 12 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff 20 Dual Bladder Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 34 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff 20 Dual Bladder Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 24 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 15 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 44 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 12 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 8 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 34 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 24 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 15 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 44 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 30 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 26 Dual Bladder Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 18 1 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable BB Tournquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceSingle USE Tourniquet Cuff 30 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff Recall (Oct 2026) – ASP GlobalASP Global, LLC.Class IIN/A
2026-10-07FDA DeviceDisposable Tourniquet Cuff 18 2 Line Recall (Oct 2026)ASP Global, LLC.Class IIN/A