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RecallWatchMedical Device Safety
Class IOngoingZ-1321-2026

Medline Industries, LP recalls Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Stee…

Medline Industries, LPNorthfield, IL, United StatesReported Feb 18, 2026 · 8 months ago
Legal News Analyst ·

Reason for recall

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

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire Steerable Electrophysiology Catheter,10 Elec. 2-5-2mm 401582RH 401940RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-10-2mm 401904RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-5-2mm 401914RH; Livewire Steerable Electrophysiology Catheter,20 Elec. 2-8-2-60-2-8-2mm 401932RH; Livewire Steerable Electrophysiology Catheter,8 Elec. 2-2-2mm 401652RH;

Lot / code information

UDI
(case) 20888277407517¿ (ea) 10888277407510 Lots EP250618 EP250630; 401940RH
UDI
10888277407480
Lot #
EP250618; 401904RH
UDI
(case) 20888277407609¿ (ea) 10888277407602 Lots EP250618 EP250630; 401914RH
UDI
(case) 20888277407524¿ (ea) 10888277407527
Lot #
EP250618; 401932RH
UDI
(case) 20888277407678¿ (ea) 10888277407671 Lots EP250618 EP250630; 401652RH
UDI
10888277407572 Lots EP250618 EP250630

What the firm is doing

On December 22, 2025, the firm issued Urgent Medical Device Recall letters as a follow-up to an earlier action in 2025 for the same issue, but newly identified item numbers and lots of previously identified item numbers. Notably, the products associated with the new/updated action are to be destroyed by the customer on-site for credit, and not returned to the manufacturer.

DistributionShow details

Distribution US nationwide.

Class IWhat this means

A reasonable probability that use of the product will cause serious adverse health consequences or death.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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