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 | BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being recalled due to the potential that a small percentage of the lot may exhibit open seals which adversely impacts unit package integrity and product sterility. |
| Product | BD Interlink threaded lock cannula This is a locking blunt plastic cannula specifically designed for IV connection to an Interlink® injection site. It is screwed down over the Interlink® injection site and a blunt plastic cannula inside the housing enters the Interlink® injection site to provide a pathway for IV fluid administration. |
| Quantity | 268,500 products |
| Distribution | Worldwide Distribution - USA (nationwide) and Internationally to Canada and Japan. |
| Initiated | 2013-11-26 |
| Classified | 2014-01-15 |
| Terminated | 2016-05-06 |
| Recall number | Z-0772-2014 |
| 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-0772-2014).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/67098/
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