• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

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

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

PANORAMIC CORP. PANORAMIC X-RAY MODEL PC-1000 Back to Search Results
Model Number 800724-1
Device Problems Component Falling (1105); Nonstandard Device (1420)
Patient Problems Contusion (1787); Fall (1848); Head Injury (1879)
Event Date 11/30/2012
Event Type  Injury  
Event Description
A recall for this issue was initiated on (b)(6) 2015.Dental assistant had a patient in the machine and was lowering it, heard a noise and it fell.Said the patient was a (b)(6) year old lady who fell to the floor with a bump on her forehead and her shoulders.She was conscious and the emt took her to hospital.
 
Manufacturer Narrative
Dental office did not provide further details on patient.(b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
PANORAMIC X-RAY MODEL PC-1000
Type of Device
PC-1000
Manufacturer (Section D)
PANORAMIC CORP.
fort wayne IN
Manufacturer Contact
4321 goshen rd.
fort wayne, IN 46818
8006542027
MDR Report Key4806107
MDR Text Key19988733
Report Number1832462-2015-00020
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 User Facility
Reporter Occupation Other
Remedial Action Repair
Type of Report Initial
Report Date 05/06/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/15/2015
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number800724-1
Device Lot Number6000 - 13885
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received11/30/2012
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured06/01/1996
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 Age78 YR
-
-