MAUDE Adverse Event Report: PANORAMIC CORP. PANORAMIC X-RAY MODEL LASER -1000; PC-1000/LASER1000

Model Number 800724-3

Device Problem Noise, Audible (3273)

Patient Problem Contusion (1787)

Event Date 10/29/2012

Event Type  Injury  

Event Description

A recall for this issue was initiated on (b)(4) 2015.Dental assistant was positioning a patient in the machine.While she was lowering the machine, it made a loud 'boom, boom' noise, slipped and struck the dental assistant.

Manufacturer Narrative

Dental office did not provide further details on the dental assistant who was struck.(b)(4).

• Brand Name: PANORAMIC X-RAY MODEL LASER -1000
• Type of Device: PC-1000/LASER1000
• Manufacturer (Section D): PANORAMIC CORP.; fort wayne IN
• Manufacturer Contact: 4321 goshen rd.; fort wayne, IN 46818 ; 8006542027
• MDR Report Key: 4806081
• MDR Text Key: 5920997
• Report Number: 1832462-2015-00006
• Device Sequence Number: 1
• Product Code: EHD
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K882436
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• 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

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: 800724-3
• Device Lot Number: 6000 - 13885
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 10/29/2012
• Initial Date FDA Received: 05/15/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 07/01/2002
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1
• Patient Outcome(s): Other