The Recall Desk
ModerateFDA (Devices)·Z-0065-2027·Announced 2026-10-07

ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, but the source text describes a labeling error regarding shelf life without reporting any illnesses, injuries, or hospitalizations. This aligns with the rubric for minor labeling errors or low-risk contamination.

Plain-English summary

ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs, model number DT-7115-02Q. The recall is due to incorrect expiration dates on products manufactured between September 2016 and March 2023. The products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

The affected lots are S1101STY, P1015STY, and N0330STY. These products were distributed nationwide in the United States, specifically in the states of MO, NV, IN, MN, GA, WI, PA, TX, CT, LA, NJ, FL, AL, NY, SC, NE, NC, OH, AZ, CO, MA, IL, KY, CA, VA, ME, KS, MD, TN, MS, AR, WA, NM, MI, and WY.

The MPR Single Use Tourniquet Cuff is a sterile disposable device used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is intended for use in surgical procedures that require the interruption of blood flow and clear visualization of the operative field. No specific instructions for consumers are provided in the source text, but the recall is classified as Class II by the FDA.

The recalled product

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…
Manufacturer
ASP Global, LLC.
Affected units
180

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (2)

  • P1015STY
  • N0330STY

Distribution

Distributed nationwide across the United States.

The notice also names 35 states specifically: