Becton Dickinson recalls Swan-Ganz Pacing Catheter model D200F7 due to potential hub leaks causing infection or blood loss. Affected units have specific model and lot numbers.
Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.
Becton Dickinson is recalling Swan-Ganz Pacing Catheters with model D200F7 because they may leak or break from the blue proximal hub, risking infection, medication loss, or blood loss. This is serious for medical use and requires immediate attention.
The catheter's blue proximal hub may leak or break due to manufacturing changes, leading to infection, medication loss, or blood loss. This happens when the hub fails under normal medical use conditions.
Healthcare professionals using Swan-Ganz Pacing Catheters with model D200F7 are most at risk. Patients receiving these catheters could face infection or blood loss if the device leaks.
Check for model D200F7 on the catheter. Affected units have specific lot numbers like D200F7-00690103147315/66725358 with an expiration date of July 2, 2027.
Immediately stop using the Swan-Ganz Pacing Catheter model D200F7 if it has the specified lot numbers.
Model D200F7 with lot numbers D200F7-00690103147315/66725358.
The affected units expire on July 2, 2027.
The recall does not mention a fix; the remedy is null.
We’ve drafted a message you can send Becton Dickinson to request your refund or repair — edit it as you like.
Subject: Recall Z-2204-2026 — Becton Dickinson Becton Dickinson Hello, I own a Becton Dickinson that is covered by recall Z-2204-2026 from Becton Dickinson. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.