The Recall Desk
ModerateFDA (Devices)·Z-0028-2027·Announced 2026-10-07

Expressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates

ASP Global is recalling Expressaire disposable tourniquet cuffs due to incorrect expiration dates. The products were labeled with a 10-year shelf life, but the 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: This is a Class II recall involving a labeling error (incorrect expiration date) without reported injuries or illnesses, fitting the criteria for a moderate severity score.

Plain-English summary

ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs, 18" x 4" 2-Line (CS 18) Red, Model A70107007. The recall involves 8,807 units manufactured between September 2016 and March 2023. The specific lot codes affected are S0922STY, S1101STY, S1214STY, R1101STY, R1201STY, Q0301STY, Q1115STY, P0325STY, P1015STY, O0120STY, N0730STY, M1230STY, and L0120STY.

The reason for the recall is that the products are labeled with a 10-year shelf life, whereas the correct validated shelf life is 5 years. This discrepancy means that some units may have been used past their intended expiration date. The FDA has classified this as a Class II recall.

The 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. Healthcare facilities and users should check their inventory for the affected model and lot codes and stop using the products if they are past the 5-year validated shelf life.

The recalled product

Product
Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 18" X 4" 2-LINE (CS 18) RED Model/Catalog Number: A70107007 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
Manufacturer
ASP Global, LLC.
Affected units
8,807

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 (12)

  • S1101STY
  • S1214STY
  • R1101STY
  • R1201STY
  • Q0301STY
  • Q1115STY
  • P0325STY
  • P1015STY
  • O0120STY
  • N0730STY
  • M1230STY
  • L0120STY

Distribution

Distributed nationwide across the United States.

The notice also names 35 states specifically:

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