Smiths Medical ASD Inc.: 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

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 21-2120-0100-02, UDI/DI 10610586040429, Serial Numbers: 1033919; REF List Number 21-2120-0100-03, UDI/DI 30610586040430, Serial Numbers: 1024307, 1024333, 1025299, 1027869, 1027794; REF List Number 21-2120-0100-50, UDI/DI 10610586038501, Serial Numbers: 1015104, 1032637, 1019622, 1019666, 1019677, 1019718, 1019720, 1019790, 1019795, 1019806, 1019812, 1019907, 1020978, 1020984, 1021003, 1021146, 1021160, 1021161, 1021229, 1021237, 1021271, 1021285, 1011594, 1011601, 1011616, 1011618, 1011638, 1011640, 1012715, 1012721, 1012726, 1012736, 1021319, 1021382, 1021393, 1023095, 1026455, 1026662, 1026793, 1027760, 1031023, 1031026, 1031696, 1032360, 1032375, 1032377, 1032381, 1032556, 1032560, 1032568, 1032569, 1032570, 1032578, 1032607, 1032633, 1034367, 1034394, 1034411, 1034412, 1034424, 1035087, 1035088, 1035103, 1035105, 1035116, 1032362, 1034083, 1035086, 1128327, 1021322, 1026791, 1034390; REF List Number 21-2120-0102-02, UDI/DI 10610586042591, Serial Numbers: 1074580, 1100001, 1099307, 1099419, 1099421, 1099440; REF List Number 21-2120-0102-03, UDI/DI 10610586042607, Serial Numbers: 1042669, 1055355, 1071360, 1074287, 1076699, 1079688, 1089683, 1054757, 1092499, 1092537, 1092547, 1092561, 1092570, 1094041, 1094824, 1099689, 1099700, 1099712, 1099716, 1099727, 1099732, 1100845, 1101619, 1102930, 1102932, 1103442, 1107615, 1107656, 1108010, 1108016, 1108388, 1113382, 1113411, 1117418, 1117437, 1121537, 1094849, 1108405; REF List Number 21-2120-0102-06, UDI/DI 10

UPC codes

10610586040429, 30610586040430, 10610586038501, 10610586042591, 10610586042607, 10610586042614, 10610586042829, 15019517084368

Source

Official record: FDA (Device enforcement) ↗

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