The FDA has posted 10 enforcement recalls of long-term greater than 30 days therapeutic intravascular catheter devices since 2025, including 2 Class I (most serious) recalls. Most recent report: Aug 5, 2026.
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients;…
Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients;…
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if ster…
Due to damage to outer tray that can potentially compromise the sterile barrier
Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to i…
Source: U.S. FDA openFDA device enforcement reports, updated continuously. Device type per the FDA's RES classification (“Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days”). Informational only — verify against the FDA before acting.