MAUDE Adverse Event Report: COLOPLAST A/S TOROSA SALINE TESTICULAR MED; SALINE FILLED TESTICULAR PROSTHESIS

Model Number	5206302400
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	02/05/2016
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence.Should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.
Event or Problem Description
According to the available information, the patient underwent removal of his left testicle due to left testicular tumor.The patient had a prosthesis placed at the time of removal.Surgeon was notified postoperatively that the implanted prosthesis had failed and had deflated.

• Brand Name: TOROSA SALINE TESTICULAR MED
• Common Device Name: SALINE FILLED TESTICULAR PROSTHESIS
• Manufacturer (Section D): COLOPLAST A/S; holtedam 1; humlebaek, da 3050 ; DA 3050
• MDR Report Key: 5873230
• Report Number: 2125050-2016-00164
• Device Sequence Number: 13459134
• Product Code: FAF
• UDI-Device Identifier: 05708932470834
• UDI-Public: 05708932470834
• Combination Product (Y/N): N
• PMA/510(K) Number: P020003
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2016
• Reporter Type: Manufacturer
• Report Source: consumer,other
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 08/12/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Physician
• Device Model Number: 5206302400
• Device Catalogue Number: 5206302400
• Device Lot Number: 4837525
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/22/2016
• Initial Report FDA Received Date: 08/12/2016
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 20 YR