WhichRecall
Class I — UrgentReported 2026-02-18

Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on GE Systems 10439072RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter Use on Siemens Systems 10438577RH; Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheter, Use on Siemens Systems 10439011RH

Recalled by Medline Industries, LP

Reason for Recall

These lots of reprocessed catheters may contain small particles of residual material

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If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025

Recall Number
Z-1324-2026
Classification
Class I
Status
Ongoing
Category
device
Initiated
2025-12-22
Reported
2026-02-18
Distribution
Distribution US nationwide.
Code Info
10439072RH UDI-DI 10197344157297 Lots EP250724 EP250808; 10439236RH UDI-DI 10197344157303 Lots EP250724 EP250808; 10438577RH UDI-DI 10197344157273 Lots EP250724 EP250808; 10439011RH UDI-DI (case) 20197344157287¿ (ea) 10197344157280¿ Lots EP250724 EP250808
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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