RACER® BILIARY XD618YFRecalls & reported problems
Medtronic, Inc. · STENT XD618YF RACER US SHORT · Class 2 · Implant
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 00613994551481), received between Oct 23, 2019 and Oct 23, 2019 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Urinary Tract Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 23, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
DURING PROCEDURE, A RACER STENT WAS IMPLANTED IN THE LEFT RENAL ARTERY. THREE DAYS POST PROCEDURE, PATIENT HAD URINARY TRACT INFECTION. PATIENT WAS TREATED WITH MEDICATION AND EVENT WAS RESOLVED. INVESTIGATOR ASSESSED EVENT IS RELATED TO THE PROCEDURE AND NOT DEVICE. NO ADDITIONAL CLINICAL SEQUELAE WAS REPORTED. PATIENT RECOVERED.
Patient problems: Urinary Tract Infection
MAUDE report 9225804 ↗
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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.
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