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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PANORAMIC CORPORATION PANORAMIC X-RAY MODEL PC-1000

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PANORAMIC CORPORATION PANORAMIC X-RAY MODEL PC-1000 Back to Search Results
Model Number 800724-1
Device Problem Migration or Expulsion of Device (1395)
Patient Problem Injury (2348)
Event Date 12/04/2015
Event Type  Injury  
Event Description
Machine came down on a patient and the patient was taken to the emergency room for evaluation.
 
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Brand Name
PANORAMIC X-RAY MODEL PC-1000
Type of Device
PC-1000
Manufacturer (Section D)
PANORAMIC CORPORATION
4321 goshen road
fort wayne IN 46818
Manufacturer (Section G)
PANORAMIC CORPORATION
4321 goshen road
fort wayne IN 46818
Manufacturer Contact
stephen yaggy
4321 goshen road
fort wayne, IN 46818
8006542027
MDR Report Key5413870
MDR Text Key37577060
Report Number1832462-2015-00073
Device Sequence Number1
Product Code EHD
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K870236
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional
Reporter Occupation Dentist
Remedial Action Replace
Type of Report Initial
Report Date 12/31/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/05/2016
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Dental Assistant
Device Model Number800724-1
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Date Manufacturer Received12/04/2015
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured08/15/2002
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
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