The Recall Desk
ModerateFDA (Devices)·Z-0029-2027·Announced 2026-10-07

ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

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 without reported injuries or illnesses are classified as Moderate.

Plain-English summary

ASP Global, LLC. is recalling approximately 12,114 units of Expressaire Disposable Tourniquet Cuffs (Model A70107008). The recall affects sterile disposable tourniquet cuffs used to wrap around a patient's limb and inflate to reduce or occlude circulation during surgery. The products were distributed nationwide in 34 states, including 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 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 lot codes are S0823STY, S1101STY, R0310STY, R0601STY, R1101STY, R1201STY, Q1115STY, P0325STY, P1015STY, N0730STY, M1230STY, and L0120STY.

Healthcare facilities and consumers should stop using the affected tourniquet cuffs and contact ASP Global, LLC. for further instructions or a refund.

The recalled product

Product
Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-LINE (CS 18) YELLOW Model/Catalog Number: A70107008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated…
Manufacturer
ASP Global, LLC.
Affected units
12,114

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 (11)

  • S1101STY
  • R0310STY
  • R0601STY
  • R1101STY
  • R1201STY
  • Q1115STY
  • P0325STY
  • P1015STY
  • N0730STY
  • M1230STY
  • L0120STY

Distribution

Distributed nationwide across the United States.

The notice also names 35 states specifically: