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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: Kits do not contain the stylet/T-lock assembly indicated as a component on the label, may lead to a procedural delay and possibly discard of the kit.

Agency Publication Date: October 23, 2020
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Affected Products

Product: Bard 3F SL PowerMidline Full Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153208

Lot Number: REEQ3598 Feb-2022 and REER0518 Mar-2022 UDI: 00801741141065

Lot Numbers:
Number
Product: Bard 3F SL PowerMidline Basic Kit CE-indicated for short term access to the peripheral venous system for selected intravenous therapies, blood sampling, and power injection of contrast media Ref: P6153118

Lot Number: REEP2920 Exp. Date: Jan-2022 UDI: 00801741141027

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 86477
Status: Resolved
Manufacturer: Becton Dickinson & Company
Manufactured In: United States
Units Affected: 2 products (45 units OUS only; 72 units)

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.