ASP Global, LLC. recalls Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18" 2 LINE
- Recalling company
- ASP Global, LLC.
- Product
- Brand Name: MPR Product Name:DISPOSABLE TOURNIQUET CUFF 18" 2 LINE (10) Model/Catalog Number: DT-7218-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
- Reason
- Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Aug 24, 2026
- Reported
- Oct 7, 2026
- Distribution
- US Nationwide distribution 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, WY.
- Status
- Ongoing
- Quantity
- 5440
- Lot / codes
- Lot Code: Model Number:DT-7218-02Q UDI-DI: UDI UDI (01) 00840001403314 All Lots produced from 01SEP2016 to 01MAR2023: S0922STY, S1101STY, R1201STY, Q1115STY, P1015STY, N0530STY
- Company location
- Austell, GA
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0066-2027
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0066-2027 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.