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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

Becton Dickinson & Company: The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.

Agency Publication Date: July 22, 2019
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Affected Products

Product: 3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

Lot Number 8303571

Lot Numbers:
Number
Product: 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061

Lot Number 8307694

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82138
Status: Resolved
Manufacturer: Becton Dickinson & Company
Manufactured In: United States
Units Affected: 2 products (460,800; 428,800)

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.