Updated AMDR Statement on Voluntary Recall of Medline Renewal Reprocessed Devices*
[Washington, D.C. — March 26, 2026] — Medline Renewal, an AMDR member, completed a voluntary recall for several of its reprocessed electrophysiology catheters and an electrosurgical product. Medline Renewal informed customers promptly to pull these products
AMDR Statement on Voluntary Recall of Medline Renewal Reprocessed Devices
[Washington, D.C. — March 8, 2026] — Patient safety is the medical device reprocessing industry’s highest priority. Regulated by the U.S. Food and Drug Administration (FDA), single use device reprocessors are subject to stringent regulation