Medical device recalls Moderate risk

MEDLINE INDUSTRIES, LP - Northfield recalls Medline procedure kits, labeled as: OL OCULAR, REF DYNJ906183K

Recall date
March 19, 2025
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-1713-2025
FDA classification
Class II
Brand / firm
MEDLINE INDUSTRIES, LP - Northfield
Sold / distributed
Worldwide distribution - US Nationwide and the countries of Panama and Canada.

Why it was recalled

It was identified that the Medline Sterile Water and Medline Sterile 0.9% Normal Saline bottles were leaking at the interface of the peel-foil and bottle opening.

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 procedure kits, labeled as: OL OCULAR, REF DYNJ906183K

Get recall alerts

Free email alert whenever MEDLINE INDUSTRIES, LP - Northfield has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: MEDLINE INDUSTRIES, LP - Northfield