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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

Sirchie Finger Print Labs Inc: Microbial Contamination of Non-Sterile Products: This is a sub-recall of H&P, Povidine Prep Pads; The Kits under recall contain Povidine Prep Pads recalled by H&P Industries due to the potential contamination with an objectionable organism, Elizabethkingia meningoseptica.; Microbial Contamination of Non-Sterile Products: This is a sub-recall of H&P, Povidine Iodine Prep Pads; The Kits under recall contain Povidine Prep Pads recalled by H&P Industries due to the pot

Agency Publication Date: August 31, 2011
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 58394
Status: Resolved
Manufacturer: Sirchie Finger Print Labs Inc
Manufactured In: United States
Units Affected: 9 products (966 kits; 2857 kits; 2851 kits; 532 kits; 3999 kits; 1200 kits; 4500 kits; 1199 kits; 630 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.