Class II
Medical Device Recall: Medline Adult Anesthesia Set, REF DYNJ39985G
Medline Industries, LP · September 10, 2025
Reason for Recall
Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.
Distribution
US Nationwide distribution in the states of MO.
States Affected
NATIONWIDE
Quantity Affected
950 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0137-2026
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.