FDA Media Alert Detail

FDA Safety Alert

Catheter Recall Expansion: Medline Industries Removes Reprocessed Electrophysiology and Ultrasound Catheters

  • U.S. Food and Drug Administration
  • September 2, 2026
  • ID: http://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/catheter-recall-expansion-medline-industries-removes-reprocessed-electrophysiology-and-ultrasound

FDA MedWatch Safety Alert

Certain reprocessed catheters may contain residual particulates that could cause infection, embolism, or thrombosis
Content syndicated from the official FDA MedWatch Safety Alerts and Adverse Event Reporting Program.
View Official Announcement on FDA.gov

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