Medical Device Recall: Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
Medline Industries, LP · July 31, 2025
Reason for Recall
Specific lots of reprocessed electrophysiology and ultrasound catheters may contain small residual particulates. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk of an inflammatory response or systemic infection, and if particulate were to dislodge during use and contact circulating blood and/or the heart, it may produce a granulomatous reaction or thrombus formation, which may lead to cerebral or pulmonary embolism, or deep vein thrombosis.
Distribution
Domestic US distribution nationwide. International distribution pending. No international distribution.
States Affected
NATIONWIDE
Quantity Affected
7913 eaches
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2613-2025
Status: ongoing
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