Reported Feb 18, 2026 · Ongoing
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters
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?
Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters
5 of 5 products
| # | Product as published |
|---|---|
| 1 | Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH |
| 2 | Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH |
| 3 | Livewire Steerable Electrophysiology Catheter,20 Elec. 2-5-2mm 401914RH |
| 4 | Livewire Steerable Electrophysiology Catheter,20 Elec. 2-8-2-60-2-8-2mm 401932RH |
| 5 | Livewire Steerable Electrophysiology Catheter,8 Elec. 2-2-2mm 401652RH |
- Lot codes and dates
- 401582RH UDI-DI (case) 20888277407517¿ (ea) 10888277407510 Lots EP250618 EP250630; 401940RH UDI-DI 10888277407480 Lot EP250618; 401904RH UDI-DI (case) 20888277407609¿ (ea) 10888277407602 Lots EP250618 EP250630; 401914RH UDI-DI (case) 20888277407524¿ (ea) 10888277407527 Lot EP250618; 401932RH UDI-DI (case) 20888277407678¿ (ea) 10888277407671 Lots EP250618 EP250630; 401652RH UDI-DI 10888277407572 Lots EP250618 EP250630
- Amount recalled
- 41
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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