Drug recall
CADD-Solis Medication Safety Software, Administrator CD, Version 3.1, REF 21-2194-0301-01. Product Usage: The…
FDA recall event 69408 · Class II · Smiths Medical ASD, Inc.
Key facts
| Event ID | 69408 |
|---|---|
| Recall numbers | Z-0166-2015 |
| Recalling firm | Smiths Medical ASD, Inc. |
| Product type | Devices |
| Products | CADD-Solis Medication Safety Software, Administrator CD, Version 3.1, REF 21-2194-0301-01. Product Usage: The CADD-Solis Medication Safety Software- Administrator allows use of a computer to create… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Smiths Medical has identified an issue with a single batch (Lot Number 2752712) of CADD"-Solis Medication Safety Software Administrator 3.1 CD s. CADD"-Solis Medication Safety Software… |
| Initiation date | Sep 29, 2014 |
| Report date | Nov 12, 2014 |
| Termination date | Feb 25, 2015 |
| City | Saint Paul |
| State | MN |
| Country | United States |
| FEI number | 2183502 |
At a glance
- 1–9 Products in this recall
- 10–99 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: