BD Interlink threaded lock cannula This is a locking blunt plastic… — Class II medical device recall Z-0772-2014
Terminated recall by Becton Dickinson & Company, reported 2014-01-22, distributed nationwide. BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being recalled due to the potential that a
| Recall number | Z-0772-2014 |
|---|---|
| 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 | 2013-11-26 |
| Classified | 2014-01-15 |
| Reported by FDA | 2014-01-22 |
| Terminated | 2016-05-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, JP |
| Quantity | 268,500 products |
| Reason classes | sterility, packaging |
| Lot numbers | 3021392 |
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.
Reason for recall
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.
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-0772-2014. 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.