Lunderquist G49227Recalls & reported problems
William Cook Europe ApS · Lunderquist, Extra Stiff Wire Guide · Class 2
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00827002492271), received between Mar 3, 2021 and Mar 17, 2021 — classified as 2 injuries.
The most frequently reported specific device problem is “Device Handling Problem” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Device Handling Problem2
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.
InjuryMar 17, 2021Device Handling Problem; Device Handling Problem
DESCRIPTION OF EVENT ACCORDING TO INITIAL REPORTER: THE TIP OF THE WIRE BROKE OFF IN THE CATHETER. THEY HAD TO SNARE THE TIP TO REMOVE IT. THEY WERE NOT ABLE TO SUCCESSFULLY MANIPULATE THE CATHETER. THE DIALYSIS IS OK AND FLOWING WHERE IT SHOULD. ADDITIONAL INFORMATION RECEIVED ON 01MAR2021: IT WAS A DIALYSIS CATHETER AND THEY HAD TO USE FORCEP TO REMOVE THE TIP OF WIRE FROM THE CATHETER. PATIENT OUTCOME: THE PATIENT DID NOT REQUIRE ANY ADDITIONAL PROCEDURES DUE TO THIS OCCURRENCE. ACCORDING TO THE INITIAL REPORTER, THE PATIENT DID NOT EXPERIENCE ANY ADVERSE EFFECTS DUE TO THIS OCCURRENCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11508171 ↗InjuryMar 3, 2021Device Handling Problem; Device Handling Problem
NO ADDITIONAL INFORMATION REGARDING THE PATIENT AND/OR EVENT HAS BEEN RECEIVED SINCE THE PREVIOUS MEDWATCH REPORT WAS SENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11403664 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.