ZINGER® SUPPORT ZNGRS180HJ (UDI 00763000569525)Recalls & reported problems
Medtronic, Inc. · GDWR ZNGRS180HJ ZINGERS 5PK 180 J HY · Class 2
All models of ZINGER SUPPORT (6)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00763000569525), received between Aug 19, 2024 and Oct 24, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Material Deformation2
- Deformation Due to Compressive Stress1
- Detachment of Device or Device Component1
- Entrapment of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 24, 2024Detachment of Device or Device Component; Material Deformation; Detachment of Device or Device Component; Material Deformation
DURING A PROCEDURE AN ATTEMPT WAS MADE TO USE TWO ZINGER GUIDEWIRES WITH A LEFT VENTRICULAR (LV) LEAD TO NAVIGATE THE CORONARY SINUS. IT WAS REPORTED THAT THE FIRST GUIDEWIRE SHREDDED DURING MANEUVERS OF THE DEVICE. THE ENTIRE GUIDEWIRE WAS SUCCESSFULLY REMOVED. THE SECOND GUIDEWIRE GOT STUCK IN THE LV LEAD AND BOTH PRODUCTS HAD TO BE REMOVED FROM THE PATIENT. ANOTHER DEVICE WAS PLACED AS THERE WAS NO CAPTURE IN THE LEFT VENTRICLE, THE LEAD WAS NOT USED. THE PATIENT IS ALIVE WITH NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20520566 ↗MalfunctionAug 19, 2024Entrapment of Device; Deformation Due to Compressive Stress; Material Deformation; Entrapment of Device; Deformation Due to Compressive Stress; Material Deformation
AN ATTEMPT WAS MADE TO USE ONE LV LEAD AND ONE ZINGER GUIDEWIRE TO PLACE A LEAD IN A NON-CALCIFIED NARROW VEIN, WITH MODERATE TORTUOSITY IN THE CORONARY SINUS. THE ZINGER GUIDEWIRE WAS INSPECTED WITH NO ISSUES. THE ZINGER GUIDEWIRE WAS PREPPED PER IFU WITH NO ISSUES. THE LESION WAS NOT PRE-DILATED. THE DEVICE DID NOT PASS THROUGH A PREVIOUSLY-DEPLOYED STENT. RESISTANCE WAS NOT ENCOUNTERED WHEN ADVANCING THE DEVICE. EXCESSIVE FORCE WAS NOT USED DURING INSERTION/DELIVERY. IT WAS REPORTED THAT THE LEAD COULD NOT BE ADVANCED IN THE NARROW VEIN. AFTER MULTIPLE ATTEMPTS, THE DECISION WAS MADE TO ABORT AND SWITCH TO LEFT BUNDLE BRANCH AREA PACING (LBBAP). WHEN THE LEAD AND WIRE WERE REMOVED FROM THE PATIENT, THE WIRE HAD FRAYED/COME APART AND COULD NOT BE REMOVED FROM THE LEAD. THE PATIENT IS ALIVE WITH NO INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19999970 ↗
Other Wire, guide, catheter devices
- HI-TORQUE BALANCE MIDDLEWEIGHT UNIVERSAL II 1009664Abbott Vascular Inc. · WIRE, GUIDE, CATHETER321 reports
- SYNCHRO 14 M00313010Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls220 reports
- PressureWire™ C12059Lightlab Imaging, Inc. · WIRE, GUIDE, CATHETER1 death296 reports
- SYNCHRO 2 M00326410Stryker Corporation · WIRE, GUIDE, CATHETER2 recalls155 reports
- ENROUTE .014" Guidewire 11686-01Silk Road Medical, Inc. · Wire, Guide, Catheter2 deaths228 reports
- ARROW IPN035915Teleflex Incorporated · WIRE, GUIDE, CATHETER217 reports
- OmniWire Pressure guide wire 89185Philips Image Guided Therapy Corporation · Wire, Guide, Catheter1 recall1 death160 reports
- ARROW IPN055780Teleflex Incorporated · Wire, guide, catheter4 recalls0 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