Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector issues that may prevent proper catheter insertion or locking.
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 with Sherlock Tip Location System (TLS) Stylet. The catheter's distal connector may be too small or deformed, causing it to not pass through the connector or lock properly. This could lead to improper catheter placement.
The distal connector may have a reduced inner diameter, making it difficult to pass the catheter through. The catch slot may also be deformed, preventing the catheter from locking securely. This could lead to improper catheter placement.
Healthcare professionals who use this catheter for central venous catheterization are likely affected. Patients receiving this catheter may be at risk if improper placement occurs.
Check for the product name 'Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F'. The UDI number (01)10801741035989 is listed on the product.
Look for the UDI number (01)10801741035989 on the catheter packaging or label.
The catheter's distal connector may have a reduced inner diameter or be deformed, causing it to not pass through the connector or lock properly.
The recall record does not specify a remedy, so contact Bard Access Systems for further instructions.
The recall indicates potential issues with the distal connector that could lead to improper placement, so it is not recommended for use without verification.
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-1659-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1659-2021 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.
