Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1705-2025 — Medline Sterile Water, USP, 100mL, REF RDI30295

U.S. FDA — Device Enforcement · United States · 2025-03-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1705-2025
Date of alert
2025-03-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10884389338230
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.