The Recall Desk
ModerateFDA (Devices)·Z-0030-2027·Announced 2026-10-07

Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates

ASP Global is recalling Expressaire disposable 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: This is a labeling error regarding shelf life without reported injuries or illnesses, fitting the criteria for a moderate severity recall.

Plain-English summary

ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs, Model A70107009, due to incorrect expiration dates on the product. The devices were 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 recall involves 5,738 units 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 affected lot codes are S0823STY, R0310STY, R0601STY, R1101STY, R1201STY, Q0301STY, Q1115STY, P0325STY, O1020STY, N0730STY, and L0120STY.

These sterile disposable tourniquet cuffs are used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. The FDA has classified this as a Class II recall. Healthcare facilities should stop using the affected devices and contact the manufacturer for instructions on return or replacement.

The recalled product

Product
Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 2-LINE (CS 18) YELLOW Model/Catalog Number: A70107009 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
5,738

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 (10)

  • R0310STY
  • R0601STY
  • R1101STY
  • R1201STY
  • Q0301STY
  • Q1115STY
  • P0325STY
  • O1020STY
  • N0730STY
  • L0120STY

Distribution

Distributed nationwide across the United States.

The notice also names 35 states specifically: