Emprint SX CA30L2NRecalls & reported problems
Covidien LP · Long Navigation Antenna with Thermosphere Technology · Class 2
All models of Emprint SX (6)
Data updated Oct 16, 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 10884521703292), received between Apr 19, 2024 and Apr 19, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Defective 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Defective Device1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 19, 2024Defective Device; Appropriate Device Problem Term/Code Not Available; Defective Device; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE REPORTER, DURING PROCEDURE, THE NAVIGATION COMPONENT DID NOT WORK AND ALL DIAGNOSTICS WERE CLEAR ON MACHINE. THE SECOND IMAGE ON THE NAVIGATION SCREEN TO THE RIGHT WAS RAPIDLY BLINKING AND UNABLE TO USE THE NAVIGATION ON THE PROCEDURE. NAVIGATION DID NOT WORK ON THE MACHINE. THE PROCEDURE WAS NOT ABLE TO BE COMPLETED, AND THE PROCEDURE WAS ABORTED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 19143743 ↗
Other SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES devices
- Emprint CA20L2Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES2 recalls1 death43 reports
- Emprint CA15L2Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES2 recalls1 death41 reports
- Emprint CA30L2Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES2 recalls2 reports
- Emprint CA15L1Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES1 recall49 reports
- Solero 700106001-USAngiodynamics, Inc. · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES92 reports
- NEUWAVE PR15XTNeuwave Medical, Inc. · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES90 reports
- Emprint CA20L1Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES1 recall18 reports
- Emprint CA30L1Covidien LP · SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES1 recall1 death9 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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