ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global, LLC. is recalling 2,600 units of 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: The recall is classified as FDA Class II, and the hazard is a minor labeling error regarding shelf life without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
ASP Global, LLC. is recalling 2,600 units of Expressaire Disposable Tourniquet Cuffs, Model 564014. The recall affects lots produced between September 1, 2016, and March 1, 2023. The specific lot codes involved are S0823STY, S0922STY, S1101STY, S1214STY, R0601STY, R1101STY, Q0301STY, N0730STY, M0130STY, M0730STY, and M0930STY.
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 labeling error could result in the use of the device beyond its validated expiration date.
The affected 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 match the recalled description.
The recalled product
- Product
- Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 44" X 4" 1-LINE (CS 10) GREEN Model/Catalog Number: 564014 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.
- Hazard
- Affected units
- 2,600
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)
- S0922STY
- S1101STY
- S1214STY
- R0601STY
- R1101STY
- Q0301STY
- N0730STY
- M0130STY
- M0730STY
- M0930STY
Distribution
Related recalls
Same manufacturer · ASP Global, LLC.
See all →- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateExpressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateFDA Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
Same hazard · mis labeling
See all →- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateAdmiral Beverage Recalls 7up Tropical Cans with Undeclared Sugar
FDA (Food) · 2026-10-07
- ModeratePercussionaire Recalls Intrapulmonary Percussive Ventilation Devices Due to Labeling Warning
FDA (Devices) · 2026-10-07
Similar recalls
- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date
FDA (Devices) · 2026-10-07
- ModerateASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateASP Global Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Date
FDA (Devices) · 2026-10-07
- ModerateExpressaire Disposable Tourniquet Cuffs Recalled for Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateFDA Recalls Expressaire Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateExpressaire Disposable Tourniquet Cuff Recalled for Incorrect Expiration Date
FDA (Devices) · 2026-10-07