FDA Warns ICU Medical Over Infusion Pump Modifications
The FDA has issued a warning letter to ICU Medical, citing regulatory violations related to unapproved modifications to two of its infusion pumps.
The FDA has issued a warning letter to ICU Medical, citing regulatory violations related to unapproved modifications to two of its infusion pumps.
Fresenius Kabi has signed a multiyear agreement under which the Mayo Clinic will purchase 10,000 Ivenix large-volume infusion pumps.
Eitan Medical announced the successful completion of sale and transition of its wearable injectors business to LTS so the company can focus on its infusion therapy solutions.
The FDA has issued a warning letter to ICU Medical, citing regulatory violations related to unapproved modifications to two of its infusion pumps.
IVX Health announced two new Connecticut infusion centers in the greater New Haven and Norwalk communities.
Read MoreIRadimed Corp. issued an Urgent Medical Device Correction Letter regarding a potential issue with some 1057 Syringe Adapter Sets.
Read MoreICU Medical announced its Plum 360 smart infusion system was recognized as the top-performing smart pump in two categories by KLAS Research.
Read MoreSmiths Medical is recalling certain computerized ambulatory delivery device (CADD) administration sets and medication cassette reservoirs—both of which are intended for use with CADD infusion pumps—for two potential issues.
Read MoreFresenius Kabi announces that its Ivenix Infusion System has been successfully implemented at San Luis Valley Health in Colorado.
Read MoreSmiths Medical has issued an Urgent Medical Device Correction Letter for two potential issues with CADDÂ infusion system infusion sets.
Read MoreB. Braun's wireless devices of the Space Infusion Pump System has earned certification to UL 2900-2-1 via the UL Cybersecurity Assurance Program.