FDA recall Z-1802-2019
Arrow International Inc · Class II · device
Product
Arrow JACC with Chlorag+ard Technology Jugular Axillo subclavian Central Catheter Product Code: CDC 42552 JX1A
Reason for recall
Lidstock states the incorrect expiration date for the product
Distribution
Nationwide Foreign:
Key facts
- Status
- Terminated
- Initiation date
- 2019-04-23
- Report date
- 2019-06-26
- Termination date
- 2021-01-13
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Reading, PA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1802-2019