MAUDE Adverse Event Report: Edwards Lifesciences PR SWAN-GANZ PACING TD CATHETER; Electrode, Pacemaker, Temporary

Model Number	D205F7
Medical Device Problem Code	Pacing Problem (1439)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/12/2026
Type of Reportable Event	Malfunction

• Brand Name: SWAN-GANZ PACING TD CATHETER
• Common Device Name: Electrode, Pacemaker, Temporary
• Manufacturer (Section D): Edwards Lifesciences PR; state rd indus pk 402 km 1.4; anasco PR 00610
• Manufacturer (Section G): Edwards Lifesciences PR; state rd indus pk 402 km 1.4; anasco PR 00610
• Manufacturer Contact: samantha eveleigh ; 17200 laguna canyon rd,; irvine, CA 92618 ; +1(949)201-7706
• MDR Report Key: 50421337
• Report Number: 2015691-2026-18018
• Device Sequence Number: 10583146
• Product Code: LDF
• UDI-Device Identifier: 00690103197334
• UDI-Public: 00690103197334
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: Preamend
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 08/24/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: D205F7
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 08/24/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Sex: Unknown