Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
REF 7617408 Recalled by Bard Access Systems Inc. Due to Catheters contain two issues: 1. the inner diameter...
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 Bard Access Systems Inc. directly.
Affected Products
REF 7617408, Groshong NXT ClearVue Catheter, Full Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035255 - Product Usage: is designed for use when central venous catheterization is prescribed.
Quantity: N/A
Why Was This Recalled?
Catheters contain two issues: 1. the inner diameter of the distal connector may be reduced resulting in inability to pass the catheter through the connector and 2. the catch slot on the distal connecter may be deformed resulting in the inability to properly lock
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Bard Access Systems Inc.
Bard Access Systems Inc. has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report