Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to Devices may have higher than expected amounts of...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact MEDLINE INDUSTRIES, LP - Northfield directly.
Affected Products
Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 401582R, 401904R, 401904R, 401905R, 401933R, and 401991R
Quantity: 74 units
Why Was This Recalled?
Devices may have higher than expected amounts of bacterial endotoxin.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About MEDLINE INDUSTRIES, LP - Northfield
MEDLINE INDUSTRIES, LP - Northfield has 822 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report