FDA recall Z-0148-2022

Smiths Medical ASD Inc. · Class II · device

Product

CADD Administration Sets, Model #21-7346-24

Reason for recall

Product may have been manufactured with an air filter assembled in an incorrect orientation.

Distribution

Canada

Key facts

Status
Terminated
Initiation date
2020-07-14
Report date
2021-10-27
Termination date
2023-08-04
Voluntary/Mandated
Voluntary: Firm initiated
Location
Minneapolis, MN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0148-2022