Asp Global, Llc.: Tourniquet, Pneumatic
ASP Global is recalling MPR brand single-use tourniquet cuffs (model DT-7024-02Q) manufactured between September 2016 and March 2023 because they were labeled with an incorrect 10-year expiration date when the actual validated shelf life is 5 years. The cuffs, which are sterile devices used to restrict blood flow during surgery, were distributed nationwide across all U.S. states. Products that have exceeded their true 5-year shelf life may no longer be sterile or effective for surgical use.
- Recalling firm
- ASP Global, LLC.
- Product
- Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 24" 2 LINE (10) Model/Catalog Number: DT-7024-02Q 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/f5dca571-ef2e-4f7c-8cf3-dd5eec71501f