The Recall Desk

FDA (Devices) recall action 82350

Becton Dickinson & Company recalled 2 products on 2019-04-17

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2019-04-17
Critical
0
Units
—

Why these products were recalled

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

The agency’s own wording, quoted from the enforcement report.

States named across these recalls

1–2 of 2

  • ModerateFDA (Devices)··2019-04-17

    Becton Dickinson Recalls Gravity IV Sets Due to Kinked Tubing

    Becton Dickinson is recalling specific lots of Gravity IV Sets with 3-port Closed Stopcock Manifolds due to a confirmed complaint trend for kinked tubing.

    Product
    Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
    Category
    Distribution
    10 states
  • HighFDA (Devices)··2019-04-17

    Becton Dickinson Recalls Gravity IV Sets Due to Kinked Tubing

    Becton Dickinson is recalling specific lots of Gravity IV Sets with 3-port Closed Stopcock Manifolds due to a confirmed complaint trend for kinked tubing.

    Product
    Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07
    Category
    Distribution
    10 states