Bard recalls Groshong NXT ClearVue Catheter with potential distal connector problems that may prevent proper catheter insertion or locking. Affected units have specific model numbers and lot codes.
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 is recalling Groshong NXT ClearVue Catheter with Sherlock Tip Location System due to two issues: the distal connector may be too narrow to pass the catheter through, and the catch slot may deform, preventing proper locking. This could lead to improper catheter placement.
The distal connector's inner diameter may be reduced, making it difficult to pass the catheter through. The catch slot may deform, causing the catheter to not lock properly. Both issues could lead to improper catheter placement.
Healthcare professionals using the catheter for central venous catheterization are most likely affected. Patients receiving this catheter treatment may also be impacted.
Check for model numbers starting with REF 69655405 and lot codes like redx4687, rees1313, or reev1270. The catheter is designed for central venous catheterization procedures.
Look for the model number REF 69655405 and lot codes such as redx4687, rees1313, or reev1270 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 for model number REF 69655405 and lot codes like redx4687, rees1313, or reev1270 on the catheter packaging.
The recall record does not specify a remedy, so contact Bard Access Systems, Inc. for guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1664-2021 — Bard Bard Hello, I own a Bard that is covered by recall Z-1664-2021 from Bard. 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.
