GOETZ™ Temporary Pacing Electrode Catheter 007157PRecalls & reported problems
C. R. Bard, Inc. · Goetz Temporary Pacing Electrode Catheter, Bipolar · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741011337), received between Aug 6, 2021 and Aug 6, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Biocompatibility” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Biocompatibility1
Patient problems
- Tissue Breakdown1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 6, 2021Biocompatibility; Biocompatibility
IT WAS REPORTED THAT ST-SEGMENT ELEVATION MYOCARDIAL INFARCTION (STEMI), STATUS POST (S/P) CARDIAC ARREST AND RECENT TAMPONADE FROM RIGHT VENTRICULAR (RV) FREE WALL RUPTURE FROM TV PACING WIRE. AROUND NOON, WHILE SPEAKING WITH THE DOCTOR THE PATIENT BECAME MORE SOMNOLENT AND WAS NOTED TO BE HYPOTENSIVE TO 60S/40S. AS THE PATIENT WAS BOLUSED WITH 1L LACTATED RINGER'S SOLUTION AND RESTARTED ON LEVOPHED, ALSO NOTED TO LOSE CONSCIOUS FOR A MINUTE AND WAS BAG VENTILATED THEN REAWAKENED. CARDIAC REMAINED SINUS. LEVOPHED WAS TITRATED UP TO 0.6 TO MAINTAIN BLOOD PRESSURE. ON POINT OF CARE ECHO, PATIENT WAS FOUND TO HAVE A PERICARDIAL EFFUSION WITH FLUID ANTERIOR TO RIGHT VENTRICLE C/F RIGHT VENTRICULAR WALL RUPTURE VS. OTHER TEAR MEASURING 1.5 CM IN DEEPEST POCKET. PATIENT THEN HAD STAT LIMITED ECHOCARDIOGRAM SHOWING PERICARDIAL EFFUSION. PATIENT HAD TAMPONADE PHYSIOLOGY AND BECAME MORE TACHYCARDIAC WITH HYPOTENSION AND PULSUS SEEN ON A LINE. STABILIZED TO SYSTOLIC BLOOD PRESSURE (SBP) IN THE 90S, DIASTOLIC BLOOD PRESSURE (DBP) 50S PER A LINE AND A LINE WAS REWIRED AT BEDSIDE. PATIENT WAS MAINTAINED ON LEVOPHED 0.6 CONTINUOUS INFUSION OF LACTATED RINGER'S BOLUS. PATIENT REMAINED CONSCIOUS,
Patient problems: Tissue Breakdown
MAUDE report 12292070 ↗
Other ELECTRODE, PACEMAKER, TEMPORARY devices
- N/A 006173PC. R. Bard, Inc. · ELECTRODE, PACEMAKER, TEMPORARY161 reports
- SWAN-GANZ D200F7Edwards Lifesciences LLC · ELECTRODE, PACEMAKER, TEMPORARY1 recall0 reports
- ETHICON TPW32Ethicon, LLC · ELECTRODE, PACEMAKER, TEMPORARY1 death46 reports
- ETHICON TPW20Ethicon, LLC · ELECTRODE, PACEMAKER, TEMPORARY39 reports
- N/A 520007PC. R. Bard, Inc. · ELECTRODE, PACEMAKER, TEMPORARY33 reports
- Pacel™ 401763St. Jude Medical Cardiovascular Division · ELECTRODE, PACEMAKER, TEMPORARY21 reports
- Pacel™ 401771St. Jude Medical Cardiovascular Division · ELECTRODE, PACEMAKER, TEMPORARY1 death16 reports
- SWAN-GANZ PACING TD CATHETER D205F7Edwards Lifesciences LLC · Electrode, Pacemaker, Temporary13 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page