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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Aspen Surgical Products, Inc.: Affected products were manufactured with materials found to have a bioburden level exceeding the limit at which the product's sterilization process was validated. As a result, the firm cannot provide full assurance that the affected products were effectively sterilized, and the product may compromise a sterile field and increase the risk of a surgical site infection.

Agency Publication Date: August 30, 2021
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Affected Products

Product: Jessie Sterile Arm Suspension Kit, Product Code 711300, (previous product code 100401), Sample Kit S711300

All lots manufactured between July 9, 2019 to July 9, 2021

Product: Marco Shoulder Stabilization Kit, Product Code 711100, (previous product code 100601), Sample Kit S711100

All lots manufactured between July 9, 2019 to July 9, 2021

Product: Norton Arm Kit, Product Code 711400, (previous product code 031001), Sample Kit S711400

All lots manufactured between July 9, 2019 to July 9, 2021

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 88476
Status: Resolved
Manufacturer: Aspen Surgical Products, Inc.
Manufactured In: United States
Units Affected: 3 products (1429; 4270; 124)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.