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Panoramic Corporation PC-4000Recalls & reported problems

Young Ps Acquisition, LLC · Unit, X-ray, Extraoral with Timer- PC-4000 · Class 2

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 00862309000347), received between Apr 10, 2017 and Apr 10, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Maintenance Does Not Comply To Manufacturers Recommendations” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Maintenance Does Not Comply To Manufacturers Recommendations1
  • Power Problem1

Patient problems

  • Electric Shock1
  • 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.

  • InjuryApr 10, 2017Maintenance Does Not Comply To Manufacturers Recommendations; Power Problem; Maintenance Does Not Comply To Manufacturers Recommendations; Power Problem

    THE (B)(6) TECH CALLED IN AND SAID ONE OF THE STAFF MEMBERS, (B)(6), GOT ZAPPED. AFTER CALLING THE OFFICE AND SPEAKING TO HER, SHE STATED THAT SHE WENT TO POWER DOWN THE MACHINE AND FELT THE BUZZ. SHE SAID IT WAS LIKE WHEN A CHILD STICKS THEIR FINGER IN A WALL OUTLET. SHE HAD SLIGHT TINGLING IN HER ARM FOR A COUPLE HOURS. SHE ALSO MENTIONED THAT THEY MADE A REPORT AT THE OFFICE AS WELL. SHE SAID SHE'S FINE. SHE JUST TOLD HER BOSS WHAT HAPPENED AND THEY CALLED THEIR TECH IN TO INVESTIGATE. FOUND OUT THE POWER SWITCH AT THE BASE OF THE MACHINE WAS BROKEN AND PER A PREVIOUS CASE ON (B)(6) 2016 THIS HAS BEEN BROKEN FOR SOME TIME. QUOTED PARTS COST BUT THE OFFICE NEVER DID THE REPAIR. NOW SOMEONE GOT SHOCKED WHILE TRYING TO PRESS THE SWITCH.

    Patient problems: Electric Shock; No Known Impact Or Consequence To Patient

    MAUDE report 6475535 ↗

Other Unit, X-Ray, Extraoral With Timer devices

All Unit, X-Ray, Extraoral With Timer devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.