Coblation K7920-01Recalls & reported problems
Smith & Nephew, Inc. · PERC DLR SPINE WAND SURGICAL DEVICE · Class 2
All models of Coblation (62)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00817470004472), received between Dec 11, 2017 and Dec 11, 2017 — classified as 1 malfunction.
The most frequently reported specific device problem is “Crack” (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 16, 2026.
Most reported problems
Device problems
- Crack1
- Defective Component1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 11, 2017Crack; Defective Component
IT WAS REPORTED THAT THE DOCTOR HAD AN ISSUE PLACING THE CANNULA. WHEN HE REMOVED IT TO REPOSITION, HE NOTICED THERE WAS A "NOTCH" OR A "DIVOT" THAT WAS PERCEIVED TO BE A CRACK AT FIRST. EITHER WAY, THE CANNULA WAS DEFECTIVE. NO PATIENT INJURY WAS REPORTED, 30 MINUTES TO 1 HOUR DELAY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7105159 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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