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HomeTACTICAL MEDICAL SOLUTIONS, LLC › SOF® TOURNIQUET NH, COLOR - RESCUE ORANGE

SOF® TOURNIQUET NH, COLOR - RESCUE ORANGE

TACTICAL MEDICAL SOLUTIONS, LLC · Model 2 · UDI-DI 00818630011545

GAX
10
510(k) clearances
89
Adverse events (2 deaths)
8
Recalls
334
Facilities

Description

Among tourniquet brands, the SOF® Tactical Tourniquet is one of the top performing medical tourniquets currently available. It is the tourniquet of choice for many of the world's most elite and experienced warriors who have selected it for its outstanding ability to control severe bleeding, high level of reliability and ease of application. While some military units have replaced their issued tourniquets with the SOF®TT, other military units (including special forces) have implemented SOP's stating that the SOF® Tactical Tourniquet is to be used on all lower extremity bleeds. That means the SOF®TT is the tourniquet trusted to control the most severe extremity hemorrhage on the battlefield. The key to successful implementation of a device to be used in a high stress environment is training and ease of use. For law enforcement officers, application of the tourniquet is similar to the use of a hobble. This existing level of familiarity reduces training time and aids in the effectiveness of the device. ADVANTAGES OF THE SOF® TACTICAL TOURNIQUET 100% Effective. Proven to be 100% effective during US Army Institute of Surgical Research testing. Simple application. Unlike other tactical medical tourniquets that require you to learn two methods of application and implement the proper method when under stress, the SOF®TT is applied the same way to an arm or leg. By accounting for the factors of human performance in combat, we have minimized the risk of failure. Applying a tourniquet should not be a multiple choice exam; It should be simple and straight forward. The SOF®TT provides the necessary effectiveness with an unmatched level of simplicity to increase the overall effectiveness of the device. Durability. The SOF®TT is constructed of quality, high-strength materials. The special forces tourniquet handle is machined from a solid piece of aircraft aluminum and maintains its strength in extreme temperatures. The tri-rings are molded Acetyl, a high impact plastic tha

Recalls

DateFirmReason
2020-12-28Mar-Med CoA failure can occur if the user attempts to remove the device by partially snipping the edge and pulling on it. The device may tear into two pieces with a portion remaining in plac
2018-05-02The Seaberg Company IncBased on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati
2018-05-02The Seaberg Company IncBased on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati
2018-05-02The Seaberg Company IncBased on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human pati
2015-08-31Pyng Medical CorporationOnce tested, it is required that the tourniquet be returned to its Ready position then placed in its packaging. Each tourniquet was tested for functionality, but in some cases, the
2014-08-05ICU Medical, Inc.ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ
2014-08-05ICU Medical, Inc.ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ
2014-08-05ICU Medical, Inc.ICU Medical is recalling the BD PosiFlush Sterile Field Saline Flush Syringe because some unit packages may exhibit open seals which impacts package sterility and potentially produ

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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.