Overview of recall records associated with Smiths Medical ASD, Inc., including dates, categories and classifications where available.
Classification mix: Class I: 5.
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…
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…
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP infusion pumps.
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…
This page summarizes recall records in which the official source identifies Smiths Medical ASD, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
