Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems that may prevent proper catheter insertion and 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 Grosh:ng NXT ClearVue Catheter with Sherlock Tip Location System because the distal connector may be too small or deformed, causing the catheter to not pass through or lock properly. This could lead to improper catheter placement and potential complications.
The distal connector may have a reduced inner diameter, making it difficult for the catheter to pass through. Additionally, the catch slot may be deformed, preventing the catheter from locking securely in place. This could result in improper catheter placement and potential complications.
Healthcare professionals who use this catheter for central venous catheterization are likely affected. Patients receiving this catheter are at risk if the catheter cannot be properly inserted or locked.
Look for the product name 'Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen' with UDI: (01)10801741035996. The product was sold with lot number reep1720.
Verify the product name, UDI code (01)10801741035996, and lot number (reep1720) to confirm if the item is recalled.
The catheter's distal connector may have a reduced inner diameter or be deformed, causing it to not pass through or lock properly.
The recall record does not specify a remedy, so check the product details to confirm if it's affected and contact Bard Access Systems for further instructions.
The recall indicates potential issues with catheter insertion and locking, but the record does not specify a risk of serious injury.
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-1660-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1660-2021 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.
