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

Published: 03/05/2026

Sources:
  • Food and Drug Administration
Relevant To:
  • Ambulatory Surgical Centers,
  • Rural Emergency Hospitals,
  • Critical Access Hospitals,
  • Hospitals,
  • Ambulatory Care

The U.S. Food and Drug Administration (FDA) is updating the communication "Catheter Recall: Medline Removes Certain Reprocessed Electrophysiology and Ultrasound Catheters" and issuing the new communication "Catheter Recall Expansion: Medline Removes Certain Reprocessed Electrophysiology and Ultrasound Catheters" to notify the public that Medline Industries has issued letters to affected customers recommending additional lots of reprocessed electrophysiology and ultrasound catheters be removed fr…

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