Reported Feb 18, 2026 · Ongoing
Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
Medline Industries, LP
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753
Is this the product you have?
- Medline ReNewal
- Reprocessed ViewFlex Xtra ICE CathetersViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
- Lot codes and dates
- UDI-DI (case) 20197344019554¿ (ea) 10197344019557 Lots
EP250324EP250416EP250512EP250521EP250609EP250630EP250710EP250724
- UDI-DI (case) 20197344019554¿ (ea) 10197344019557 Lots
- Amount recalled
- 650
This recall covers 20 products
The agency filed one notice per product. You are reading one of them; the other 19 are below.
7 more are in the archive.
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
These lots of reprocessed catheters may contain small particles of residual material. 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
Using this product could cause serious injury, illness or death — stop using it now.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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