Sonopet iQ 550025B317Recalls & reported problems
Stryker Corporation · 12cm iQ 120 Claw · Class U
All models of Sonopet iQ (16)
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 07613327422504), received between Aug 9, 2024 and Aug 9, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Overheating of Device” (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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Overheating of Device1
Patient problems
- Muscle Weakness/Atrophy1
- Nerve Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 9, 2024Overheating of Device; Adverse Event Without Identified Device or Use Problem; Overheating of Device; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED POSTOPERATIVE, THE PATIENT EXPERIENCED SENSORY LOSS IN LEFT L3 AREA, THIGH MUSCLE WEAKNESS, DUE TO DAMAGE CAUSED DURING USE OF THE SONOPET IQ TIP. IT WAS FURTHER REPORTED THAT THE PATIENT IS DOING WELL, AND SENSORY LOSS HAS RETURNED. IT WAS ALSO REPORTED THAT THE ORIGINAL PROCEDURE FOR L2/3 LAMINECTOMY, LEFT HERNIOTOMY, WAS COMPLETED SUCCESSFULLY, WITH NO MEDICAL INTERVENTION OR DELAYS.
Patient problems: Muscle Weakness/Atrophy; Nerve Damage
MAUDE report 19950799 ↗
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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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