FDA Device recall Z-1813-2015
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measu…
- FDA Device
- Class II
- terminated
- Published 2015-06-24
On 2015-06-24 the FDA classified a Class II recall of CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measu… by Smiths Medical Asd, citing smiths Medical has become aware of an issue with an intermittent occurrence of binding of the locking assembly on some CADD¿-Solis pumps. Binding of the Cassette/ Keypad Lock can….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1813-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-05-26 |
| Published | 2015-06-24 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Smiths Medical Asd |
| Distribution | US |
Product
CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.
Reason
Smiths Medical has become aware of an issue with an intermittent occurrence of binding of the locking assembly on some CADD¿-Solis pumps. Binding of the Cassette/ Keypad Lock can occur after latching the CADD¿-Solis Medication Cassette Reservoir or Administration Set disposable to the pump. When binding occurs, it can prevent the key from fully rotating the Cassette/ Keypad Lock to the locked (e
Identifiers
| code_info | Serial Number US 1061044 1061058 1061072 1061075 1061082 1061083 1061093 1061104 1061105 1061106 1061107 10…Serial Number US 1061044 1061058 1061072 1061075 1061082 1061083 1061093 1061104 1061105 1061106 1061107 1061108 1061109 1061110 1061111 1061112 1061113 1061114 1061115 1061116 1061117 1061118 1061119 1061120 1061121 1061122 1061123 1061124 1061125 1061126 1061127 1061128 1061129 1061130 1061131 1061132 1061133 1061134 1061135 1061136 1061137 1061138 1061139 1061140 1061141 1061142 1061143 1061144 1061145 1061146 1061147 1061148 1061149 1061150 1061151 1061152 1061153 1061154 1061155 1061156 1061157 1061158 1061159 1061160 1061161 1061162 1061163 1061164 1061165 1061166 1061167 1061168 1061169 1061170 1061171 1061172 1061173 1061174 1061175 1061176 1061177 1061178 1061179 1061180 1061181 1061182 1061183 1061184 1061185 1061186 1061187 1061188 1061189 1061190 1061191 1061192 1061193 1061194 1061195 1061196 1061197 1061198 1061199 1061200 1061201 1061202 1061203 1061204 1061205 1 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1813-2015%22
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