Advanced practice providers have the opportunity to instill hope in patients through education and personalized care.

The company has asked users to monitor patients frequently to ensure the appropriate infusion is being delivered.

Baxter’s recall of the system involves updating instructions for use. It does not require removal from use or sale. However, ...

As radiopharmaceutical therapies gain momentum, new challenges are emerging in how they’re administered—especially around ...

Smiths Medical has issued a Class I recall for certain CADD-Solis and CADD-Solis VIP ambulatory infusion pumps due to multiple issues that could interrupt or delay medication delivery. The FDA ...

The Food and Drug Administration issued Class I recalls, the most serious type, for two Smiths Medical infusion pumps due to the potential for serious injury or death.

The FDA issued three notices identifying warnings sent out by ICU Medical's Smiths Medical unit related to infusion pump problems.

Ingersoll Rand Inc. IR recently completed the acquisition of Lead Fluid (Baoding) Intelligent Equipment Manufacturing Co., ...

Smiths Medical also identified three issues associated with the potential for thermal damage in affected infusion pumps. If certain parts of the pump are damaged, heat can melt the plastic housing to ...

Smiths has not reported any serious injuries or deaths related to the issues, but the FDA sees a risk of harm.

I n today’s hyper-connected healthcare environment, the supply chain has quietly become one of the sector’s most vulnerable ...