Asp Global, Llc.: Tourniquet, Pneumatic
Recall Summary ASP Global is recalling MPR brand single-use tourniquet cuffs (model DT-7108-02Q) manufactured between September 2016 and March 2023 because they are labeled with a 10-year shelf life when the actual validated shelf life is only 5 years. These sterile devices are used during surgery to reduce blood flow to a patient's limb, and the incorrect expiration dates mean some units may no longer be sterile or effective. The affected products were distributed nationwide across most U.S. states.
- Recalling firm
- ASP Global, LLC.
- Product
- Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 8" 2 LINE (10) Model/Catalog Number: DT-7108-02Q 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 I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-08-24
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fce6846c-3b8c-4b17-aace-229a9e13442b