FDA Device recall Z-2420-2024

CADD-Solis VIP ambulatory Infusion Pumps, Model 2110

FDA Device
Class I
ongoing
Published 2024-08-14

On 2024-08-14 the FDA classified a Class I recall of CADD-Solis VIP ambulatory Infusion Pumps, Model 2110 by Smiths Medical Asd, citing the CADD Solis VIP Ambulatory Infusion Pump is indicated for the following uses: " For intravenous, intraarterial, subcutaneous, intraperitoneal, perineural, surgical site, epidur….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2420-2024
Classification	Class I
Status	ongoing
Initiated	2024-02-27
Published	2024-08-14
Last updated	2026-09-13 11:57 UTC
Company	Smiths Medical Asd
Distribution	n/a

Product

CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. 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

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.

Identifiers

code_info	REF List Number 21-2111-0100-00, UDI/DI 10610586039195, Serial Numbers: 10610586039195; REF List Number 21-2111-0100… REF List Number 21-2111-0100-00, UDI/DI 10610586039195, Serial Numbers: 10610586039195; REF List Number 21-2111-0100-51, UDI/DI 30610586039205, Serial Numbers: 1008871, 1011314, 1011695, 1012140, 1012157, 1012387, 1012393, 1012430, 1012607, 1012611, 1012749, 1012751, 1012752, 1012758, 1012765, 1012767, 1012769, 1012773, 1012815, 1012988, 1013182, 1013185, 1013186, 1013187, 1013219, 1013221, 1013223, 1013230, 1013235, 1013237, 1013239, 1013251, 1013256, 1013264, 1013265, 1013278, 1013282, 1013291, 1013295, 1013301, 1013562, 1013817, 1013824, 1013853, 1013866, 1013953, 1013979, 1014000, 1014064, 1014103, 1014117, 1014279, 1014282, 1014288, 1014302, 1014308, 1014447, 1014463, 1016862, 1016876, 1016881, 1014804, 1014806, 1014811, 1014831, 1014844, 1014861, 1014880, 1014895, 1015034, 1015375, 1015382, 1016292, 1016522, 1016709, 1038360, 1016879, 1016927, 1016961, 1023905, 1016989, 1016990, 1017003, 1017005, 1017006, 1017049, 1017051, 1017075, 1017096, 1017143, 1017146, 1017159, 1017161,

code_info

REF List Number 21-2111-0100-00, UDI/DI 10610586039195, Serial Numbers: 10610586039195; REF List Number 21-2111-0100…

REF List Number 21-2111-0100-00, UDI/DI 10610586039195, Serial Numbers: 10610586039195; REF List Number 21-2111-0100-51, UDI/DI 30610586039205, Serial Numbers: 1008871, 1011314, 1011695, 1012140, 1012157, 1012387, 1012393, 1012430, 1012607, 1012611, 1012749, 1012751, 1012752, 1012758, 1012765, 1012767, 1012769, 1012773, 1012815, 1012988, 1013182, 1013185, 1013186, 1013187, 1013219, 1013221, 1013223, 1013230, 1013235, 1013237, 1013239, 1013251, 1013256, 1013264, 1013265, 1013278, 1013282, 1013291, 1013295, 1013301, 1013562, 1013817, 1013824, 1013853, 1013866, 1013953, 1013979, 1014000, 1014064, 1014103, 1014117, 1014279, 1014282, 1014288, 1014302, 1014308, 1014447, 1014463, 1016862, 1016876, 1016881, 1014804, 1014806, 1014811, 1014831, 1014844, 1014861, 1014880, 1014895, 1015034, 1015375, 1015382, 1016292, 1016522, 1016709, 1038360, 1016879, 1016927, 1016961, 1023905, 1016989, 1016990, 1017003, 1017005, 1017006, 1017049, 1017051, 1017075, 1017096, 1017143, 1017146, 1017159, 1017161,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2420-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.