Smiths Medical ASD, Inc.

Devices and FDA recall records listed on MedWatcher for Smiths Medical ASD, Inc..

What MedWatcher tracks

This page covers the devices and recall records listed below, not the complete product catalogue or recall history. A recall may apply only to specific models, lots, or serial numbers.

Tracked devices: 1
Recall records: 3
Source records last checked: Oct 27, 2026

Manufacturer names

Device and manufacturer names are linked using official product, UDI, or FDA records. The source links below show the supporting information.

Official records may use a legal name, brand, division, or shortened name. Similar names do not necessarily refer to the same manufacturer.

Smiths Medical ASD, Inc.Source-name variantOfficial source (opens in a new tab)

Sources used for this page

U.S. Food and Drug AdministrationFDA medical device recall event 96620Last checked Aug 16, 2026 U.S. Food and Drug AdministrationFDA medical device recall event 96624Last checked Aug 16, 2026 U.S. Food and Drug AdministrationFDA medical device recall event 96628Last checked Aug 16, 2026

Infusion pumps

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Medfusion 4000 Syringe Infusion Pump

Smiths Medical ASD, Inc. · Infusion pumps

No linked recall records

Latest source check Oct 8, 2026

Recent recall records

Class I recallOngoing

CADD Solis HSPCA Pump recall — FDA event 96628

Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.

FDA · FDA event 96628Posted May 7, 2025

Class I recallOngoing

CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: recall — FDA event 96620

Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm under certain conditions, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.

FDA · FDA event 96620Posted May 7, 2025

Class I recallOngoing

CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4 recall — FDA event 96624

There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.

FDA · FDA event 96624Posted May 5, 2025

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Recent recall records

Class I recallOngoing

CADD Solis HSPCA Pump recall — FDA event 96628

Pumps may experience Wireless Connection Modules intermittent connection alarms, which will interrupt an active infusion. Interruption or delay of therapy can lead to serious patient injury or death.

FDA · FDA event 96628Posted May 7, 2025

Class I recallOngoing

CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: recall — FDA event 96620

FDA · FDA event 96620Posted May 7, 2025

Class I recallOngoing

CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4 recall — FDA event 96624

There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.

FDA · FDA event 96624Posted May 5, 2025

Smiths Medical ASD, Inc.

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What MedWatcher tracks

Manufacturer names

Sources used for this page

Infusion pumps

Medfusion 4000 Syringe Infusion Pump

Recent recall records

CADD Solis HSPCA Pump recall — FDA event 96628

CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: recall — FDA event 96620

CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4 recall — FDA event 96624

Smiths Medical ASD, Inc.

Follow Smiths Medical ASD, Inc.

What MedWatcher tracks

Manufacturer names

Sources used for this page

Infusion pumps

Medfusion 4000 Syringe Infusion Pump

Recent recall records

CADD Solis HSPCA Pump recall — FDA event 96628

CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: recall — FDA event 96620

CADD-Solis Infusion Pump Models: 1) PUMP KIT, CADD-SOLIS, MDL 2110, V4 recall — FDA event 96624