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