CADD Administration Sets — Class II medical device recall Z-0148-2022
Terminated recall by Smiths Medical ASD Inc., reported 2021-10-27. Product may have been manufactured with an air filter assembled in an incorrect orientation.
| Recall number | Z-0148-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smiths Medical ASD Inc., Minneapolis, MN, United States |
| Recall initiated | 2020-07-14 |
| Classified | 2021-10-19 |
| Reported by FDA | 2021-10-27 |
| Terminated | 2023-08-04 |
| Countries outside the US | CA |
| Quantity | 371 units |
| Lot numbers | 3750848, 3766764, 3776356, 3776357, 3793886, 3793887, 3793888, 3796141, 3847669 |
| Model numbers | 21-7346-24 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0148-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.