Panoramic Corporation CCD EncompassRecalls & reported problems
Young Ps Acquisition, LLC · System, X-ray, Extraoral Source, Digital Encompass · Class 2
Data updated Oct 18, 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 00862309000361), received between Jun 13, 2018 and Jun 13, 2018 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (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.
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Fire1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 13, 2018Electrical /Electronic Property Problem; Fire; Electrical /Electronic Property Problem; Fire
THE APS TECHNICIAN, (B)(6), WAS AT THE OFFICE WORKING ON THE MACHINE AND REPLACED CABLE 58 ON THE MACHINE. WHEN THE MACHINE WAS POWERED ON, THE CAPACITOR BOARD STARTED CRACKLING AND THEN BURST INTO FLAMES. THE TECHNICIAN HAD TO PUT THE FIRE OUT WITH HIS SWEATER. THE APS TECHNICIAN WAS NOT PHYSICALLY INJURED.
Patient problems: No Patient Involvement
MAUDE report 7598029 ↗
Other Unit, X-Ray, Extraoral With Timer devices
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- Schick/XIOS AE 100008286Sirona Dental, Inc. · Unit, X-Ray, Extraoral With Timer3 reports
- Panoramic Corporation PC-4000Young Ps Acquisition, LLC · Unit, X-Ray, Extraoral With Timer1 report
- Schick AE 100006036Sirona Dental, Inc. · Unit, X-Ray, Extraoral With Timer1 report
- FocusPaloDEx Group Oy · Unit, X-Ray, Extraoral With Timer1 report
- Schick AE 100007049Sirona Dental, Inc. · Unit, X-Ray, Extraoral With Timer1 report
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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