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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

Karl Storz Endoscopy: During a complaint investigation it was determined that an error was observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect. If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guarante

Agency Publication Date: March 20, 2020
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Affected Products

Product: Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

All Lots

Product: Karl Storz, Model # 11161C2, Flexible Neuroscope

All Lots

Product: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE, Model # 11005BC1

All Lots

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84896
Status: Active
Manufacturer: Karl Storz Endoscopy
Manufactured In: United States
Units Affected: 3 products (73 scopes; 42 scopes; 21 scopes)

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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.