Recall
FDAHealthApril 8, 2026

Becton, Dickinson and Company — Swan-Ganz Pacing Catheter, Models: D200F7;

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
April 8, 2026

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, MA, NC, MN, NY, AZ, AL, LA, CO, OK, HI, MS, IL, OH, NE, DC, KS, NV, WI, SD, IA, AR, ID, OR, WY, MT, RI, VT, DE, AK, NH, ND, ME, PR and the countries of Japan, Brazil, Colombia, Australia, New Zealand, Poland, Czech Republic, South Africa, Mauritius, Germany, Israel, Iran, Slovakia, Switzerland, Slovenia, Bulgaria, Cyprus, Saudi Arabia, United Arab Emirates (UAE), Kuwait, Malta, Bahrain, Qatar, Hungary, Morocco, Romania, Lebanon, Tunisia, Oman, Turkey, Austria, Belgium, Luxembourg, France, Netherlands, Italy, Spain, Canary Islands, Portugal, United Kingdom, Northern Ireland, Ireland, Denmark, Sweden, Iceland, Norway, Estonia, Finland, Greece, Chile, Puerto Rico, Canada.

What's affected?

Product
Swan-Ganz Pacing Catheter, Models: D200F7;
Lot code
(Expiration):

Additional details

Model-UDI-DI/Lot(Expiration): D200F7-00690103147315/66725358(7/2/2027)

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 53.

View original FDA notice →

Get Health recall alerts

Delivered to your inbox. Free. No account required.