HIGHFDA DEVICE

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

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.

Becton, Dickinson andHealth & Personal CareMedical DevicesModel-UDI-DI(Expiration): SGPT755P/00690103219388/65869018(6/24/2026)66010501(9/23/2026)67122784(10/28/2027)

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
April 8, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
April 8, 2026
Hazard Level
HIGH
Brand
Becton, Dickinson and
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Becton, Dickinson and
Model numbers
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
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    April 8, 2026

  2. Reported by FDA DEVICE

    May 27, 2026

  3. RecallRadar source check

    June 3, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Becton, Dickinson and Company or your healthcare provider for instructions

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Full Description

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.. Classification: Class II. Quantity: 183. Distribution: 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.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
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
Affected States
ALL
Report Date
May 27, 2026
Recall Status
ACTIVE