FDA Device recall Z-0148-2022
CADD Administration Sets, Model #21-7346-24
- FDA Device
- Class II
- terminated
- Published 2021-10-27
On 2021-10-27 the FDA classified a Class II recall of CADD Administration Sets, Model #21-7346-24 by Smiths Medical Asd, citing product may have been manufactured with an air filter assembled in an incorrect orientation.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0148-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-07-14 |
| Published | 2021-10-27 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Smiths Medical Asd |
| Distribution | n/a |
Product
CADD Administration Sets, Model #21-7346-24
Reason
Product may have been manufactured with an air filter assembled in an incorrect orientation.
Identifiers
| code_info | Lot Numbers: 3750848, 3776357, 3793886, 3766764, 3793887, 3796141, 3776356, 3793888, 3847669 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0148-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.