ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global, LLC. is recalling 30 units of MPR 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 involves a labeling error regarding shelf life. No illnesses, injuries, or deaths are reported in the source text, fitting the criteria for a moderate severity voluntary precautionary recall.
Plain-English summary
ASP Global, LLC. is recalling 30 units of MPR Disposable Tourniquet Cuffs, model DB-7018-01Q. The recall involves sterile disposable tourniquet cuffs intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. The affected units 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 was initiated because the products are labeled with a 10-year shelf life, whereas the correct validated shelf life is 5 years. The affected units were manufactured between September 2016 and March 2023. Specific lot codes identified in the recall are N0330STY and Q1115STY.
Healthcare facilities and consumers who have these specific products should stop using them and contact ASP Global, LLC. for further instructions or a return. The recall is classified as Class II by the FDA.
The recalled product
- Product
- Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 20" DUAL BLADDER, 1 LINE (10) Model/Catalog Number: DB-7018-01Q 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
- 30
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 (1)
- Q1115STY
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 MPR Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateFDA Recalls MPR Disposable Tourniquet Cuffs Due to Incorrect Expiration Date
FDA (Devices) · 2026-10-07
- ModerateASP Global Recalls Tourniquet Cuffs Due to Incorrect Expiration Dates
FDA (Devices) · 2026-10-07
- ModerateRecall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Date
FDA (Devices) · 2026-10-07
- ModerateFDA Recalls MPR 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