medical MODERATE Updated 2026-10-07

ASP Global, LLC. recalls Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15"

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Recalled Product

Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE (10) Model/Catalog Number: DT-7115-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No

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Hazard / Issue

Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot Code: Model Number:DT-7115-02Q UDI-DI: UDI UDI was not applicable at time of manufacture. All Lots produced from 01SEP2016 to 01MAR2023: S1101STY, P1015STY, N0330STY

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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