The Recall Desk
ModerateFDA (Devices)·Z-0053-2027·Announced 2026-10-07

MPR Single Use Tourniquet Cuffs Recalled for Incorrect Expiration Dates

ASP Global is recalling 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 and involves a labeling error regarding shelf life. Per the rubric, minor labeling errors and voluntary precautionary recalls are typically scored as Moderate (2).

Plain-English summary

ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs, model DT-7024-01Q. The recall affects 1,740 units manufactured between September 2016 and March 2023. The products were distributed nationwide in 34 states, including Missouri, Nevada, Indiana, and California.

The recall was initiated because the products are labeled with a 10-year shelf life, whereas the correct validated shelf life is 5 years. This discrepancy means the expiration dates printed on the packaging are incorrect. The tourniquet cuffs are sterile, disposable devices used to wrap around a patient's limb and inflate to reduce or occlude circulation during surgery.

Healthcare facilities and consumers should stop using these specific tourniquet cuffs and contact ASP Global, LLC. for further instructions. The affected lot codes are S1101STY, R1201STY, Q0301STY, Q1115STY, P1015STY, and N0330STY.

The recalled product

Product
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24" 1 LINE (10) Model/Catalog Number: DT-7024-01Q 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…
Manufacturer
ASP Global, LLC.
Affected units
1,740

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 (5)

  • R1201STY
  • Q0301STY
  • Q1115STY
  • P1015STY
  • N0330STY

Distribution

Distributed nationwide across the United States.

The notice also names 35 states specifically:

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