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

Recall Z-0172-2025 — Medline AMBULATORY MINI PACK, REF DYNJ82579; medical procedure convenience kit

U.S. FDA — Device Enforcement · United States · 2024-09-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0172-2025
Date of alert
2024-09-04
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)
40195327198153
Reported risk: It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the pouch is opened/unsealed.
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.