Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
BALLARD* Multi-Access Port Catheter Recalled by Avanos Medical, Inc. Due to Product was distributed with incorrect expiration date.
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Avanos Medical, Inc. directly.
Affected Products
BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use
Quantity: 6,280 devices (314 cases)
Why Was This Recalled?
Product was distributed with incorrect expiration date.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Avanos Medical, Inc.
Avanos Medical, Inc. has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report