WhichRecall
Class I — UrgentReported 2026-02-18

Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿

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-1323-2026
Classification
Class I
Status
Ongoing
Category
device
Initiated
2025-12-22
Reported
2026-02-18
Distribution
Distribution US nationwide.
Code Info
UDI-DI (case) 20197344019554¿ (ea) 10197344019557 Lots EP250324 EP250416 EP250512 EP250521 EP250609 EP250630 EP250710 EP250724
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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