Class II

Medical Device Recall: Medline procedure kits, labeled as: HAND, REF DYNJ902002J

MEDLINE INDUSTRIES, LP - Northfield · March 19, 2025

Reason for Recall

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.

Distribution

Worldwide distribution - US Nationwide and the countries of Panama and Canada.

States Affected

NATIONWIDE

Quantity Affected

159 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1714-2025

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.

MEDLINE INDUSTRIES, LP - Northfield Medical Device Recall: Medline procedure kits, labeled as: HAND, REF DYNJ902002J | SafeCheck