Bard Access Systems recalls Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to distal connector problems 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 Grosh:ng NXT ClearVue Catheter with Sherlock Tip Location System because the distal connector may not allow proper catheter insertion or locking. This could lead to improper catheter placement or disconnection during medical procedures.
The distal connector may have a reduced inner diameter, making it difficult to pass the catheter through. Additionally, the catch slot may deform, preventing the catheter from locking securely in place.
Healthcare professionals using the catheter for central venous catheterization are most at risk. Patients receiving this catheter as part of medical treatment may also be affected.
Check for the model number REF 9617408D on the catheter packaging. The product was sold with lot numbers reen4697 and reep0632.
Verify the model number REF 9617408D and lot numbers reen4697 or reep0632 on the catheter packaging.
The distal connector may have a reduced inner diameter, making it difficult to pass the catheter through, and the catch slot may deform, preventing proper locking.
Check the model number and lot numbers on the packaging to confirm if it is recalled. Bard Access Systems has not provided a specific remedy for this recall.
The recall addresses 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-1662-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1662-2021 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.
