CADD-Solis VIP ambulatory Infusion Pumps — Class I medical device recall Z-2421-2024
Ongoing recall by Smiths Medical ASD Inc., reported 2024-08-14. The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarter
| Recall number | Z-2421-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smiths Medical ASD Inc., Minneapolis, MN, United States |
| Recall initiated | 2024-02-27 |
| Classified | 2024-08-02 |
| Reported by FDA | 2024-08-14 |
| UPC / GTIN / UDI-DI | 10610586038501, 10610586038891, 10610586040429, 10610586042591, 10610586042607, 10610586042614, 10610586042829, 15019517084368, 15019517096378, 15019517096385, 15019517096392, 15019517126587, 15019517126594, 15019517126600, 15019517126617, 15019517149999, 15019517150001, 15019517150292, 15019517150568, 30610586040430 |
| Serial numbers | 01162016, 0557, 1002021, 1002071, 1002084, 1002112, 1002116, 1003554, 1003921, 1003922, 1003931, 1004354, 1004408, 1004529, 1004534, 1004596, 1004690, 1004721, 1004752, 1004757, 1004771, 1004790, 1007860, 1007973, 1008715 and 475 more |
| Model numbers | 2120 |
Product
CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and 21-2127 ) Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an intraoperative site, epidural space or subarachnoid space. Therapies that require a continuous rate of infusion, intermittent bolus, and/or with patient-controlled demand doses.
Reason for recall
The CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidural space, or subarachnoid space infusion.
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-2421-2024. 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.