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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 Drug

Cooperative Workshops Inc: Microbial Contamination of Non-Sterile Products: Kits were manufactured using a recalled component (alcohol pads).

Agency Publication Date: March 3, 2011
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 57614
Status: Resolved
Manufacturer: Cooperative Workshops Inc
Manufactured In: United States
Units Affected: 13 products (48/50-pad boxes Item 16063 and 3/10-pad boxes of Item 160400; 22 kits; 4 kits; 19 kits; 42 kits; 1,500 kits (Part 25019); 17 kits (Part 25020); 475 kits; 2,451 kits; 7 kits; 413 kits; 20,000 kits (Model 2000000464); 30,000 kits (model 20000001786); and 29,976 kits (model 20000002993); 9,976 kits; 3 kits)

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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.