Medium RiskFDA Device

Becton Dickinson & Company: The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.

Agency Publication Date: April 10, 2019

Affected Products

Product: Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07

18105594 18105595 18105596 18105597

Product: Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07

18105828 18105830 18105857 18105858

Additional Information

Agency: Food and Drug Administration (FDA)

Event ID: 82350

Status: Resolved

Manufacturer: Becton Dickinson & Company

Manufactured In: United States

Units Affected: 2 products (21220 total cases of 20)

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.