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

Recall Z-1528-2025 — Brand Name: Ballard Product Name: Closed Suction Catheters Model/Catalog Number: 22714183-5 Software Version: N/A Product Description: Ballard Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE, MDI Component: N/A

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

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1528-2025
Date of alert
2025-03-19
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Avanos Medical, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00609038982649
Reported risk: Lack of sterility assurance for closed suction catheter systems
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.