FDA Flags Three Infusion Pump Corrections from Smiths Medical as Class I Recalls
Issues may cause therapy delays, false alarms, or thermal damage, though no injuries reported to date.
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Medical Device Recall Volume Hits Three-Year Low, But Class I Events Rise
While total recalls and units affected declined in Q1 2025, the number of Class I events increased.
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New Data Tool Tracks Country of Origin to Spot Healthcare Tariff Risk
ECRI’s tool helps health systems identify products affected by tariffs and find safe, functionally equivalent alternatives to maintain supply continuity.
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How RTLS Helps Hospitals Reduce Medical Equipment Search Time
Hospitals are implementing real-time location systems to speed up equipment retrieval and minimize disruptions that interfere with patient care.
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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.
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