Bard Access Systems recalls Groshong NXT ClearVue Catheter kits due to distal connector problems that may prevent proper catheter insertion or locking. Affected units have specific UDI and lot numbers.
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
Bard Access Systems is recalling Groshong NXT ClearVue Catheter kits because the distal connector may not allow the catheter to pass through properly or lock securely. This could lead to improper catheter placement during medical procedures.
The catheter's distal connector has two issues: its inner diameter may be too small to pass the catheter through, and the catch slot may be deformed, preventing proper locking. This could cause improper catheter placement during medical procedures.
Healthcare professionals using the catheter for central venous catheterization are most at risk. Patients receiving this catheter treatment may also be affected.
Check for the UDI code (01)10801741200592 and lot numbers listed in the recall notice. The product is a 4F, Single-Lumen, 60 cm catheter kit used for central venous catheterization.
Identify the UDI code (01)10801741200592 and lot numbers listed in the recall notice.
The distal connector may have an inner diameter too small to pass the catheter through or a deformed catch slot that prevents proper locking.
The recall notice does not specify a remedy, so check the product details to confirm if it is affected and contact Bard Access Systems for further instructions.
The recall indicates potential issues with proper insertion and locking, so it is not recommended for use until the problem is resolved.
We’ve drafted a message you can send Bard Access Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-1653-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1653-2021 from Bard Access Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
