MPR Single Use Tourniquet Cuff Recalled for Incorrect Expiration Date
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
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 due to a labeling error regarding shelf life, which fits the rubric for minor labeling errors or low-risk contamination without reported injuries.
Plain-English summary
ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs, model DT-7030-02Q, due to incorrect expiration dates on the product. The affected units were manufactured between September 2016 and March 2023. The products are currently labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.
The recall involves 820 units distributed nationwide in the United States. The specific states affected include 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 affected lot codes are S1101STY, R1201STY, Q1115STY, O1020STY, N0330STY, N0530STY, and N0730STY.
Healthcare facilities and consumers should check their inventory for these specific lot codes and model numbers. If the product is found, it should be removed from use and returned to the manufacturer or disposed of according to local regulations. The FDA has classified this as a Class II recall, indicating that use of the product could cause temporary or medically reversible health consequences.
The recalled product
- Product
- Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q 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…
- Manufacturer
- ASP Global, LLC.
- Hazard
- Affected units
- 820
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 (6)
- R1201STY
- Q1115STY
- O1020STY
- N0330STY
- N0530STY
- N0730STY
Distribution
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