Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates
ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the 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: This is a labeling error regarding shelf life (FDA Class II) without reported injuries or illnesses, fitting the criteria for a moderate severity recall.
Plain-English summary
ASP Global, LLC. is recalling 80 units of MPR Single Use Tourniquet Cuffs, model number DT-7112-02Q. These sterile, disposable medical devices are intended to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgical procedures.
The recall was initiated because the products, manufactured between September 2016 and March 2023, are labeled with a 10-year shelf life. However, the correct validated shelf life for these devices is 5 years. The affected units were distributed nationwide in 33 states, including California, Texas, and New York.
Healthcare facilities and consumers should stop using the affected tourniquet cuffs immediately. Users should verify the expiration date on the packaging and contact ASP Global, LLC. for further instructions or a replacement if the product is within the 5-year validated shelf life window.
The recalled product
- Product
- Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE (10) Model/Catalog Number: DT-7112-02Q 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.
- Affected units
- 80
Distribution
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