Class II
Medical Device Recall: Medline ReNewal Reprocessed Livewire Steerable Electrophysiology Catheters, Medline Item Numbers: 401582R, 401904R, 401904R, 401905R, 401933R, and 401991R
MEDLINE INDUSTRIES, LP - Northfield · February 6, 2025
Reason for Recall
Devices may have higher than expected amounts of bacterial endotoxin.
Distribution
US Nationwide distribution in the states of AR, AZ, CA, CO, IA, IL, KS, OR, TN, TX, WA, and WI.
States Affected
NATIONWIDE
Quantity Affected
74 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1460-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.