FDA Device recall Z-1121-2019
Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
- FDA Device
- Class II
- terminated
- Published 2019-04-17
On 2019-04-17 the FDA classified a Class II recall of Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07 by Becton Dickinson And, citing the firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1121-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-05 |
| Published | 2019-04-17 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | AL, CA, DC, FL, LA, MD, NE, TN, VA, WA |
Product
Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
Reason
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
Identifiers
| code_info | 18105828 18105830 18105857 18105858 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1121-2019%22
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