Medical device recalls Moderate risk

Becton Dickinson & Company recalls Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07

Recall date
March 5, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1120-2019
FDA classification
Class II
Brand / firm
Becton Dickinson & Company
Sold / distributed
Distributed to accounts in AL, CA, DC, FL, LA, MD, NE, TN, VA, and WA.

Why it was recalled

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

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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