Santa Ana, CA, United States
Codan US Corporation recalls
1 recall recorded since 2018, most recently on 12 September 2019. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)0
Terminated or completed1
Class I (FDA)0
Terminated Class II Medical devices
- Recall started
- 12 September 2019
- Terminated
- 28 April 2021
- Reason
- Individual packages of connectors may have incomplete or bad seals which would compromise sterility.
- Distribution
- Distribution was made to CA, MI, NY, PA, and VA. There was no military/government distribution. Foreign distribution was made to Canada, Australia, New Zealand, and Chile.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2433-2020
- 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.
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.