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Serious recall: Injury is possible or has been reported. Take action promptly.

Becton, Dickinson and Company 2026-05-27 Health serious FDA
Health · FDA · Recall #FDA-Z-2203-2026

Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P Recall

Issued May 27, 2026 · Becton, Dickinson and Company

In May 2026, Becton, Dickinson and Company recalled the Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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.

What you should do

  1. 1 Stop using Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Becton, Dickinson and Company to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Becton, Dickinson and Company
Category
Health
Recall date
May 27, 2026
Units affected
Not reported
Sold at
Worldwide - US Nationwide distribution including in the states of TX, SC, CT, GA, VA, MO, NM, UT, NJ, CA, FL, PA, IN, TN, WA, KY, MD, WV, MI
Recall number
FDA-Z-2203-2026
Made in
United States
Issuing agency
FDA

In context

  • Becton, Dickinson and Company has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 356th Health recall we've logged in 2026.
Read the official FDA notice

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