Class II — Becton Dickinson & Company
| Recalling firm | Becton Dickinson and Company |
|---|---|
| Registered facility | View this company's 36 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The firm has initiated a recall due to a confirmed complaint trend for kinked tubing on the specified lots of the product. |
| Product | Gravity IV Set with 3-port Closed Stopcock Manifold Model CS42522E-07 |
| Quantity | 21220 total cases of 20 |
| Distribution | Distributed to accounts in AL, CA, DC, FL, LA, MD, NE, TN, VA, and WA. |
| Initiated | 2019-03-05 |
| Classified | 2019-04-10 |
| Terminated | 2020-07-15 |
| Recall number | Z-1120-2019 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Becton Dickinson & Company (Z-1120-2019).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82350/
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