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U.S. Department of Health and Human Services

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

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PANORAMIC CORPORATION PANORAMIC X-RAY PC-1000 Back to Search Results
Model Number 800724-1
Device Problem Migration or Expulsion of Device (1395)
Patient Problem Head Injury (1879)
Event Date 08/31/2016
Event Type  Injury  
Event Description
The machine was being adjusted downward when it fell.It is reported that the child patient received a head injury, was taken to the hospital, given medicine, released and that there were no serious injury.
 
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Brand Name
PANORAMIC X-RAY 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
tammy shiffler
4321 goshen road
fort wayne, IN 46818
8006542027
MDR Report Key5976481
MDR Text Key55584005
Report Number1832462-2016-00015
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,user faci
Reporter Occupation Other Health Care Professional
Remedial Action Repair
Type of Report Initial
Report Date 09/24/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received09/26/2016
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 Received09/01/2016
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured08/15/2006
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) Hospitalization; Other;
Patient Age9 YR
Patient Weight86
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