Medical device recalls Moderate risk

Medline Industries, LP recalls Medline Adult Anesthesia Set, REF DYNJ39985G

Recall date
September 10, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0137-2026
FDA classification
Class II
Brand / firm
Medline Industries, LP
Sold / distributed
US Nationwide distribution in the states of MO.

Why it was recalled

Specific items and lots of Medline Kits may contain Clearlink IV Sets which Baxter recalled due to customer reports of leaking.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Medline Adult Anesthesia Set, REF DYNJ39985G

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