RecallRadar

FDA Device recall Z-2203-2026

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

On 2026-05-27 the FDA classified a Class II recall of Swan-Ganz Jr Catheter, Models: SGPT54, SGPT64P, SGPT755P by Becton Dickinson And, citing 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 b….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2203-2026
ClassificationClass II
Statusongoing
Initiated2026-04-08
Published2026-05-27
Last updated2026-09-13 11:58 UTC
CompanyBecton Dickinson And
DistributionUS

Product

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

Reason

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.

Identifiers

code_info
Model-UDI-DI(Expiration): SGPT755P/00690103219388/65869018(6/24/2026), 66010501(9/23/2026), 67122784(10/28/2027); SGPT…Model-UDI-DI(Expiration): SGPT755P/00690103219388/65869018(6/24/2026), 66010501(9/23/2026), 67122784(10/28/2027); SGPT54/00690103219289/65956343(8/19/2026); SGPT64P/00690103219371

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2203-2026%22

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