Drug recall
CADD Administration Sets, Model #21-7346-24
FDA recall event 88730 · Class II · Smiths Medical ASD Inc.
Key facts
| Event ID | 88730 |
|---|---|
| Recall numbers | Z-0148-2022 |
| Recalling firm | Smiths Medical ASD Inc. |
| Product type | Devices |
| Products | CADD Administration Sets, Model #21-7346-24 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Product may have been manufactured with an air filter assembled in an incorrect orientation. |
| Initiation date | Jul 14, 2020 |
| Report date | Oct 27, 2021 |
| Termination date | Aug 4, 2023 |
| City | Minneapolis |
| State | MN |
| Country | United States |
| FEI number | 3012307300 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: