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CS 2200Recalls & reported problems

Carestream Dental LLC · CS 2200 110V/205CM LONG WALL MTD · Class 2

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 60192155153594), received between Dec 3, 2021 and Dec 3, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unintended Application Program Shut Down” (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

  • Unintended Application Program Shut Down1

Patient problems

  • Swelling/ Edema1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 3, 2021Unintended Application Program Shut Down; Unintended Application Program Shut Down

    A CS 2200 UNIT ARM FELL WHILE IN USE AND BUMPED A PATIENT. THE PATIENT WAS NOT SERIOUSLY INJURED AND DID NOT REQUIRE ANY MEDICAL ATTENTION. THE UNIT WAS MANUFACTURED IN 2016 AND INSTALLED IN MARCH 2016. THE UNIT WAS INSTALLED USING A PASSTHROUGH INSTALLATION. FROM THE PHOTOGRAPHIC EVIDENCE IT APPEARS THE HOUSING MAY HAVE BEEN FILED DOWN DURING INSTALLATION. NO MAINTENANCE WAS PERFORMED ON THE UNIT AS RECOMMENDED IN THE INSTALLATION AND SERVICE GUIDE (SM762)_ED06) OVER THE LIFE OF THE UNIT.

    Patient problems: Swelling/ Edema

    MAUDE report 12924567 ↗

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.