MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE HEART CABG CDS, REF CDS983376R

Recall date

August 28, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0119-2025

FDA classification

Class II

Brand / firm

MEDLINE INDUSTRIES, LP - Northfield

Sold / distributed

US Nationwide distribution.

Why it was recalled

Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.

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 HEART CABG CDS, REF CDS983376R