Medline Industries, LP: Device Recall

Recall #Z-2613-2025 · 07/31/2025

Class I: Dangerous

Recall Details

Recall Number
Z-2613-2025
Classification
Class I
Product Type
Device
Recalling Firm
Medline Industries, LP
Status
Ongoing
Date Initiated
07/31/2025
Location
Northfield, IL, United States
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
7913 eaches

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.

Product Description

Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH

Distribution Pattern

Domestic US distribution nationwide. International distribution pending. No international distribution.

Other Recalls by Medline Industries, LP

View all recalls by Medline Industries, LP →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.