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

Recall date

April 8, 2026

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2204-2026

FDA classification

Class II

Brand / firm

Becton, Dickinson and Company

Sold / distributed

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…

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Swan-Ganz Pacing Catheter, Models: D200F7;