Smiths Medical ASD, Inc.

Smiths Medical ASD, Inc. appears in MedWatcher through reviewed canonical device identities and source-backed FDA or official manufacturer records.

What MedWatcher tracks

This page includes only canonical device families and FDA recall events separately reviewed for publication by MedWatcher. It is not a complete product catalogue.

Reviewed device families: 1
Matched recall actions: 3
Source records last checked: Oct 8, 2026

Manufacturer identity and source matching

Canonical identity is based on the linked official product, UDI, or FDA recalling-firm source. Source-name variants are retained as aliases rather than separate manufacturer pages.

Source databases can use a legal name, brand, division, or shortened name. MedWatcher retains the form used as evidence rather than treating every similar name as the same manufacturer.

Smiths Medical ASD, Inc.Source-name variantReviewed openFDA recalling-firm identity — FUS-265Evidence 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

Page reviewed Aug 17, 2026 by MedWatcher project owner — FUS-265 · Next review by Nov 15, 2026.

Infusion pumps

View category

Medfusion 4000 Syringe Infusion Pump

Smiths Medical ASD, Inc. · Infusion pumps

No recall records found

Last checked Aug 17, 2026

Recent recall records

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

FDA · FDA event 96620Posted May 7, 2025

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 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.

Follow Smiths Medical ASD, Inc.

What MedWatcher tracks

Manufacturer identity and source matching

Sources used for this page

Infusion pumps

Medfusion 4000 Syringe Infusion Pump

Recent recall records

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

CADD Solis HSPCA Pump recall — FDA event 96628

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 identity and source matching

Sources used for this page

Infusion pumps

Medfusion 4000 Syringe Infusion Pump

Recent recall records

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

CADD Solis HSPCA Pump recall — FDA event 96628

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