Z-1682-2025Class I

CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL...

Name: Z-1682-2025 CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL...
Creator: Smiths Medical ASD, Inc.
Published: 2025-04-10
License: https://open.fda.gov/license/

Abbott Medical / initiated 2025-04-10 / Open, Classified

FDA source

Smiths Medical ASD, Inc. began a recall of CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA, Model Number: 21-2127-0105-01; 2) PUMP... on 2025-04-10. FDA classified it as Class I and gives the reason as "There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps". As of 2026-09-10, the recall status on record is Open, Classified.

Recall record

Recall number: Z-1682-2025
Classification: Class I
Status: Open, Classified
Initiated: 2025-04-10
Posted: 2025-05-05
Recalling firm: Abbott Medical
Product: CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE, 1/EA, Model Number: 21-2127-0105-01; 2) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD ENABLED, 1/EA, Model Number: 21-2120-0105-01; 3) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH 1/EA, Model Number: 21-2120-0103-01; 4) PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH 1/EA, Model Number: 21-2120-0102-51; 5) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, PHARMGUARD ENABLED 1/EA, Model Number: 21-2120-0104-01; 6) PUMP KIT, CADD-SOLIS VIP, MDL 2120, CE GLOBAL ENGLISH 1/EA, Model Number: 21-2120-0103-51; 7) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, MANUAL MODE 1/EA, Model Number: 21-2127-0104-01; 8) PUMP KIT, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER, NA ENGLISH, PHARMGUARD, 1/EA, Model Number: 21-2120-0105-00; 9) PUMP, CADD-SOLIS VIP, MDL 2120, TRIAL/LOANER CE GLOBAL ENGLISH 1/EA, Model Number: 21-2120-0103-78; 10) PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, TRIAL/LOANER 1/EA, Model Number: 21-2120-0102-78; 11) PUMP, CADD-SOLIS VIP, MDL 2120, NFHU, NA ENGLISH, PHARMGUARD ENABLED 1/EA, Model Number: 21-2120-0104-231; 12) PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, NFHU 1/EA, Model Number: 21-2120-0102-249; 13) PUMP, CADD-SOLIS VIP, MDL 2120, NFHU CE GLOBAL ENGLISH 1/EA, Model Number: 21-2120-0103-249; 14) PUMP KIT, CADD-SOLIS VIP, MDL 2120, NA ENGLISH, FACTORY LIBRARY 1/EA, Model Number: 21-2125-0104-01; 15) PUMP, CADD-SOLIS VIP, MDL 2120, ENGLISH, NFHU 1/EA, Model Number: 21-2120-0102-249.
Product code: FRN Pump, Infusion
Reason for recall: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
FDA root cause: Under Investigation by firm
Action: An URGENT MEDICAL DEVICE CORRECTION dated 4/10/25 was sent to customers. Actions for Users: Inform all affected CADD-Solis and CADD-Solis VIP users of this notice. Provide the instructions below: 1. Ensure all users or potential users of these products are immediately made aware of this notification. 2. Upon receipt of this notification and ongoing during regular maintenance, visually inspect the external condition of the battery pack or Wireless Communication Module and look for evidence of any physical damage. Handle a damaged device with caution. As stated in the battery pack Instructions for Use, if the battery pack housing is cracked or otherwise damaged, replace the battery pack. NEVER use a battery pack that appears damaged. A rechargeable battery pack must be replaced with either another CADD-Solis rechargeable battery pack or with 4 AA batteries. 3. Visually inspect the condition of the battery compartment for evidence of any physical damage. Contact Technical Support for repairs. 4. Always check the battery compartment for fluid or debris before inserting the batteries, and do not allow any fluid or debris to fall into the battery compartment. 5. Complete the electronic Response Form via the link provided within this email notification within ten days of receipt to acknowledge your understanding of this notification, even if you do not have the affected product. 6. DISTRIBUTORS: If you have distributed potentially affected products to your customers, please immediately forward your customer list to Sedgwick at [email protected]. Sedgwick will notify customers with email addresses via email and will send physical notifications to customers without email addresses in order for them to complete the Response Form Follow up Actions by Smiths Medical: Smiths Medical is continuing to investigate this matter to determine if additional actions may be warranted. For further inquiries, please contact Smiths Medical using the following information: Smit
Quantity in commerce: 313,676 items
Distribution: Worldwide - US Nationwide distribution.
Product codes and lots: All serial numbers. 1 ) 21-2127-0105-01 , UDI-DI: 15019517150292 ; 2 ) 21-2120-0105-01 , UDI-DI: 15019517150001 ; 3 ) 21-2120-0103-01 , UDI-DI: 15019517084368 ; 4 ) 21-2120-0102-51 , UDI-DI: 10610586042829 ; 5 ) 21-2120-0104-01 , UDI-DI: 15019517126587 ; 6 ) 21-2120-0103-51 , UDI-DI: 15019517096378 ; 7 ) 21-2127-0104-01 , UDI-DI: 15019517126600 ; 8 ) 21-2120-0105-00 , UDI-DI: 15019517149999 ; 9 ) 21-2120-0103-78 , UDI-DI: 15019517096392 ; 10 ) 21-2120-0102-78 , UDI-DI: 10610586042836 ; 11 ) 21-2120-0104-231 , UDI-DI: 15019517126617 ; 12 ) 21-2120-0102-249 , UDI-DI: 10610586042843 ; 13 ) 21-2120-0103-249 , UDI-DI: 15019517096385 ; 14 ) 21-2125-0104-01 , UDI-DI: 15019517126594 ; 15 ) 21-2120-0102-249 , UDI-DI: 10610586042843 ;

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-1682-2025
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-1681-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-05-14	2025-05-06
Z-1682-2025	Class I	Ongoing	Voluntary: Firm initiated	2025-05-14	2025-05-06

Product code FRN

K111275Class IICadd Solis Vip Ambulatory Infusion Pump and Cadd Solis Medication Safety SoftwareSmiths Medical Asd, Inc. / cleared 2013-02-01

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)