FDA recall Z-1244-2020

Arrow International Inc · Class II · device

Product

Arrow EPIDURAL NEEDLE COMPONENT AN-05505

Reason for recall

Product lidstock contains the incorrect expiration date for the product

Distribution

Nationwide Foreign: AT, AU, DE, CA, CZ, GT, NZ, PL, SK, and ZA

Key facts

Status
Terminated
Initiation date
2019-12-20
Report date
2020-02-26
Termination date
2021-02-25
Voluntary/Mandated
Voluntary: Firm initiated
Location
Reading, PA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1244-2020