Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System due to distal connector problems that may prevent catheter insertion or proper 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 3CG Tip Positioning System (TPS) Stylet Tip, Basic Kit, 4F. The catheter may have a reduced inner diameter or deformed catch slot at the distal connector, causing inability to 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 to pass the catheter through. Additionally, the catch slot could be deformed, preventing the catheter from locking securely. This could lead to improper placement and potential complications during medical procedures.
Healthcare professionals using the catheter for central venous catheterization are most at risk. Patients receiving this catheter treatment may experience improper placement if the device fails to lock correctly.
Check for the product name 'Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet Tip, Basic Kit, 4F'. The lot numbers listed include redx0702 through reex3469. The product was sold with CE 2797 certification.
Identify the product by checking the lot numbers listed in the recall notice: redx0702, redx1450, redx2338, redx4128, reep0823, reeq3588, reer1040, reer3480, rees0567, rees1246, rees2299, reew1849, reew4279, reex0353, reex3469.
The catheter may have a reduced inner diameter at the distal connector, causing inability to pass through, or a deformed catch slot that prevents proper locking.
Check the product details against the listed lot numbers to determine if it is affected. If it is, contact Bard Access Systems for further instructions.
The recall notice does not specify a remedy or fix for this issue.
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-1665-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1665-2021 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.
