Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07 — Class II medical device recall Z-1121-2019
Terminated recall by Becton Dickinson & Company, reported 2019-04-17, distributed in AL, CA, DC, FL, LA, MD, NE, TN…. The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of
| Recall number | Z-1121-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2019-03-05 |
| Classified | 2019-04-10 |
| Reported by FDA | 2019-04-17 |
| Terminated | 2020-07-15 |
| Distributed | AL, CA, DC, FL, LA, MD, NE, TN, VA, WA |
| Model numbers | CM42500E-07 |
Product
Gravity IV Set with 3-port Closed Stopcock Manifold Model CM42500E-07
Reason for recall
The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1121-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.