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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

TELEFLEX MEDICAL INC: The products are being recalled due to reports of breakage broke at the point of a welded joint either prior to use during setup or during use inside the patient's mouth.

Agency Publication Date: February 7, 2020
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Affected Products

Product: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

Product Code 004551003; Lot Numbers 1811331, 1902331, 1904331

Lot Numbers:
004551003
Numbers
Product: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System

Product Code 004551004; Lot Numbers 1812341, 1903341

Lot Numbers:
004551004
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84702
Status: Resolved
Manufacturer: TELEFLEX MEDICAL INC
Manufactured In: United States
Units Affected: 2 products (338,928 (199,018 US and 139,910 OUS) for all products)
Agency Last Updated: February 25, 2020

Were You Affected by This Recall?

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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.