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FDA (Device enforcement)Recalled 2024-02-27class i

Smiths Medical ASD Inc.: CADD-Solis VIP ambulatory Infusion Pumps, Model 2110. Indicated for the following uses: Intra-arterial, subcutaneous, intraperitoneal, in close proximity to nerves, into an in

Hazard

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.

Details from the source

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. Distribution: Worldwide Lot/code info: 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, 1017163, 1017172, 1017173, 1017174, 1017175, 1017180, 1017189, 1017200, 1017202, 1017221, 1017230, 1017237, 1017241, 1017244, 1017252, 1017261, 1017264, 1017267, 1017276, 1017284, 1017286, 1017290, 1017293, 1017294, 1017295, 1017302, 1017325, 1017327, 1017332, 1017333, 1017339, 1017347, 1017359, 1017407, 1017431, 1017433, 1017435, 1017436, 1017444, 1017447, 1017448, 1017455, 1017463, 1017471, 1017486, 1017488, 1017491, 1017493, 1017508, 1017509, 1017511, 1017512, 1017514, 1017516, 1017518, 1017522,

UPC codes

10610586039195, 30610586039205, 30610586039397, 10610586039416, 10610586039430, 10610586038792, 10610586038778, 10610586038891, 10610586038938, 10610586038969, 10610586039010, 10610586039065, 10610586038839, 10610586041037, 35019517135323, 35019517128677

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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