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.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a medical device defect (kinked tubing) that poses a risk of harm, but the source text does not report any specific injuries or illnesses.
Plain-English summary
Becton Dickinson & Company has initiated a recall of Gravity IV Sets with 3-port Closed Stopcock Manifold, Model CS42522E-07. The recall covers 21,220 total cases of 20 units. The affected product codes are 18105594, 18105595, 18105596, and 18105597.
The firm initiated this recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product. The agency has classified this as a Class II recall.
The product was distributed to accounts in Alabama, California, the District of Columbia, Florida, Louisiana, Maryland, Nebraska, Tennessee, Virginia, and Washington. Consumers and healthcare facilities should check their inventory for these specific product codes and stop using the affected units.
The recalled product
- Product
- Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07
- Manufacturer
- Becton Dickinson & Company
- Category
- Medical Device — IV Sets
- Hazard
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- 18105594 18105595 18105596 18105597
Distribution
Part of a larger recall action
This product is one of 2 recalled by Becton Dickinson & Company under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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