Bard recalls Groshong NXT ClearVue Catheter kits with potential connector issues that could prevent catheter passage or secure locking. Affected units have specific lot numbers and UDI 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 kits due to two connector problems: one may prevent catheter passage through the connector, and the other may cause improper locking. This could lead to failed catheter placements or complications during medical procedures.
The distal connector's inner diameter may be too small to pass the catheter through, and the catch slot may deform, preventing proper locking. This could lead to failed catheter placements or complications during medical procedures.
Healthcare professionals using these catheters for central venous catheterization are most at risk. Patients receiving these catheters through medical facilities may also be affected.
Check for the product name 'Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm' with the UDI code (01)10801741035279. Affected units have specific lot numbers listed in the recall notice.
Look for the UDI code (01)10801741035279 and lot numbers listed in the recall notice to confirm if your catheter is affected.
The catheter has two issues: the inner diameter of the distal connector may be too small to pass the catheter through, and the catch slot may deform, preventing proper locking.
Check for the UDI code (01)10801741035279 and lot numbers listed in the recall notice, which include specific codes like reds2369, reds3369, and others.
The recall does not specify a remedy, so contact Bard Access Systems, Inc. for guidance on next steps.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1656-2021 — Bard Bard Hello, I own a Bard that is covered by recall Z-1656-2021 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.
