Bard Access Systems recalls replacement connectors for 4F Groshong NXT clearVue PICC catheters due to potential fit 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 replacement connectors for certain 4F Groshong NXT clearVue PICC catheters. The connectors may have reduced inner diameter or deformed catch slots, which could prevent the catheter from passing through or locking properly.
The catheter may not pass through the connector due to a reduced inner diameter, or the connector may not lock properly because of a deformed catch slot. This could lead to catheter dislodgement or improper placement.
Healthcare professionals using the recalled connectors for central venous catheterization are most at risk. Patients receiving these catheters could experience complications if the connector fails to lock properly.
Check for the product code REF 7812400 on the connector. The catheter is designed for use with central venous catheterization and has specific lot numbers listed in the recall notice.
Identify the connector using the product code REF 7812400 and the listed lot numbers to confirm if it is recalled.
The connectors may have a reduced inner diameter or deformed catch slot, which could prevent the catheter from passing through or locking properly.
The official recall notice does not specify a remedy or action for the affected connectors.
Yes, the recall includes lot numbers such as redr1671, reds4453, and others listed in the product details.
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-1658-2021 — Bard Access Systems Bard Access Systems Hello, I own a Bard Access Systems that is covered by recall Z-1658-2021 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.
