MAUDE Adverse Event Report: OAKWORKS, INC., OAKWORKS MEDICAL CFPM 300 IMAGING TABLE

Model Number CFPM 300

Device Problem Unintended Movement (3026)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Date 12/17/2015

Event Type  malfunction  

Event Description

(b)(6) from (b)(6) called in and said that dr.(b)(6) has a patient stuck on the table in the up position.(b)(6) called the doctor and the foot pedal was stuck under the table.There is no patient harm or adverse event.

• Brand Name: OAKWORKS MEDICAL CFPM 300 IMAGING TABLE
• Type of Device: IMAGING TABLE
• Manufacturer (Section D): OAKWORKS, INC.,; 923 east wellspring rd; new freedom PA 17349
• Manufacturer (Section G): OAKWORKS, INC.,; 923 east wellspring rd; new freedom PA 17349
• Manufacturer Contact: stephen mckinley ; 923 east wellspring rd; new freedom, PA 17349
• MDR Report Key: 6660067
• MDR Text Key: 78192425
• Report Number: 2529571-2017-00010
• Device Sequence Number: 1
• Product Code: IXR
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: N/A
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 06/06/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/22/2017
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: CFPM 300
• Device Catalogue Number: 75208-T01
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 12/17/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/07/2015
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1