Customer Communications and Clinical Bulletins
Customer Communications include the latest customer letters and updates regarding ICU Medical products. These documents are organized in date descending order. Specific Clinical Bulletins can be accessed separately. For additional information, please refer to specific contact information in the individual letter or, for general inquiries, contact ICU Medical.
| Release Date | Product | Title | ICU Medical Reference |
|---|---|---|---|
| April 10 2025 | CADD-Solis™ and CADD-Solis VIP™ Ambulatory Infusion Pumps Thermal Damage | Urgent Medical Device Correction | Customer Letter (FA2503-01) |
| April 10 2025 | CADD-Solis™ Ambulatory Infusion Pumps and Wireless Communication Module | Urgent Medical Device Correction | Customer Letter (FA2503-02) |
| April 10 2025 | CADD-Solis™ and CADD-Solis VIP™ Ambulatory Infusion Pumps USO Alarm | Urgent Medical Device Notification | Customer Letter (FA2503-03) |
| July 17 2024 | CADD-Solis™ Li-ion Rechargeable Battery Packs | Urgent Medical Device Correction | Customer Letter (FA2406-02) |
| June 26 2024 | CADD™ Medication Cassette Reservoirs | Urgent Medical Device Recall | Customer Letter (FA2406-01) |
| June 26 2024 | CADD-Solis™ AC Adapter | Urgent: Medical Device Correction | Customer Letter (FA2404-05) |
| February 27 2024 | CADD-Solis™ Ambulatory Infusion Pumps | Urgent: Medical Device Correction | Customer Letter (FA2402-04) |
Rx Only. For safe and proper use, refer to the Instructions for Use.
Product(s) may not be licensed or available for sale in all countries. Please consult a product catalog, your sales representatives, or customer support for country-specific product availability. Please see the Instructions for Use for a complete listing of the indications, contraindications, warnings, and precautions. Always follow the Instructions/Directions for Use.
The information contained in this website is intended for healthcare professionals only.
