Fresh Recalls

Becton recalls

4 recent recalls on record for Becton in connected official government data as of October 22, 2026 at 12:00 PM UTC.

Models with recalls

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code (1)Swan-Ganz Catheter (1)Swan-Ganz Jr Catheter (1)Swan-Ganz Pacing Catheter (1)

All Becton recalls

FDA Class II · Medical device · September 30, 2026

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code recall — Becton, Dickinson and Company

Due to incorrect switching of Channel 1 and 2 on the module and flag labels on the tissue oximetry cables.

Official ID Z-3250-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Swan-Ganz Pacing Catheter recall — Becton, Dickinson and Company

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 bl…

Official ID Z-2204-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Swan-Ganz Jr Catheter recall — Becton, Dickinson and Company

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 bl…

Official ID Z-2203-2026 · Official record ↗

FDA Class II · Medical device · May 27, 2026

Swan-Ganz Catheter recall — Becton, Dickinson and Company

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 bl…

Official ID Z-2202-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 12:00 PM UTC.