Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K111275 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CADD-Solis VIP ambulatory infusion pump, Model Numbers: a. 21-2120-0105-02L b. 21-2120-0105-03L c... | 1 | 10/19/2021 |
FEI # 3012307300 Smiths Medical ASD Inc. |
| CADD-Solis VIP ambulatory Infusion Pumps, Model 2120 (21-2120, 21-2125, and 21-2127) Indicated... | 1 | 08/03/2024 |
FEI # 3012307300 Smiths Medical ASD Inc. |
| CADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-212... | 1 | 05/07/2025 |
FEI # 3012307300 Smiths Medical ASD, Inc. |
| CADD-Solis Li-ion Rechargeable Battery Packs, REF 21-2160-XX, which are also sold as a component of ... | 1 | 10/31/2024 |
FEI # 3012307300 Smiths Medical ASD Inc. |
| CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH... | 1 | 05/05/2025 |
FEI # 3012307300 Smiths Medical ASD, Inc. |
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