ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Date
ASP Global, LLC. is recalling 240 units of Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.
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. The hazard is a labeling error regarding shelf life, which is a minor labeling error without reported injuries or illnesses, fitting the Moderate severity criteria.
Plain-English summary
ASP Global, LLC. is recalling 240 units of Expressaire Disposable Tourniquet Cuffs, Model A70107001. The affected products are sterile, non-invasive devices intended to be wrapped around a patient's limb and inflated to reduce or occlude circulation during surgery.
The recall was initiated due to an incorrect expiration date on the product. The devices were manufactured between September 2016 and March 2023 and are labeled with a 10-year shelf life. However, the correct validated shelf life for these products is 5 years.
The affected units were distributed nationwide in the United States, specifically 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, and WY. The specific lot codes for the affected units are R1201STY and Q0301STY. Users should stop using these products and contact the recalling firm for instructions.
The recalled product
- Product
- Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8" X 2.5" 2-LINE (CS 12) LIGHT BLUE Model/Catalog Number: A70107001 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and…
- Manufacturer
- ASP Global, LLC.
- Hazard
- Affected units
- 240
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 (1)
- Q0301STY
Distribution
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