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Smiths Medical ASD Inc. Recall: CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-

Smiths Medical ASD Inc. Recall: CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21- is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Smiths Medical ASD Inc.; Product: CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 ( 21-2120 , 21-2125 , and 21-2127 ) Indicated for the follow

Recalling firmSmiths Medical ASD Inc.
ProductCADD-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 recallThe 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.
ClassificationClass I (most serious — reasonable probability of serious health consequences or death)
StatusOngoing
DistributionWorldwide
Recall initiated20240227
Recall numberZ-2421-2024
Categorydevice
StateMN
CountryUnited States

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