CODAN SWAN-LOCK Swabable Needlefree Connector — Class II medical device recall Z-2433-2020
Terminated recall by Codan US Corporation, reported 2020-07-08, distributed in CA, MI, NY, PA, VA. Individual packages of connectors may have incomplete or bad seals which would compromise sterility.
| Recall number | Z-2433-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Codan US Corporation, Santa Ana, CA, United States |
| Recall initiated | 2019-09-12 |
| Classified | 2020-06-26 |
| Reported by FDA | 2020-07-08 |
| Terminated | 2021-04-28 |
| Distributed | CA, MI, NY, PA, VA |
| Countries outside the US | AU, CA, CL, NZ |
| Quantity | 34,776 units |
| Reason classes | sterility |
| Lot numbers | 78503 |
| Model numbers | 16.7220, BC1000N |
Product
CODAN SWAN-LOCK Swabable Needlefree Connector, Catalog #BC1000N, REF 16.7220, individually packaged, 504/case, Sterile. The firm name on the label is CODAN US CORPORATION, Santa Ana, CA.
Reason for recall
Individual packages of connectors may have incomplete or bad seals which would compromise 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-2433-2020. 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.