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UNKNOWN SALINE IMPLANTS Adverse Event — Injury (MDR 1645337-2020-05888)

UNKNOWN SALINE IMPLANTS Adverse Event — Injury (MDR 1645337-2020-05888) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN SALINE IMPLANTS; Generic name: PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE; Manufacturer: MENTOR TEXAS.

DeviceUNKNOWN SALINE IMPLANTS
Generic namePROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE
ManufacturerMENTOR TEXAS
Report number1645337-2020-05888
Event typeInjury
Date received2020-04-27
Report sourceCONSUMER
NarrativeAT THE TIME OF THIS REPORT, MENTOR HAS RECEIVED NO INFORMATION REGARDING EXPLANTATION OR AN EXPECTED EXPLANTATION DATE. IT IS UNKNOWN AT THIS TIME IF THE DEVICE WILL BE MADE AVAILABLE FOR RETURN. AS A RESULT, NO PRODUCT FAILURE ANALYSIS CAN BE CONDUCTED, AND NO DETERMINATION OF POSSIBLE CONTRIBUTING FACTORS CAN BE MADE. AS SUCH, THE INVESTIGATION WILL BE CLOSED. IF THE COMPLAINT DEVICE IS RECEIVED
SourceopenFDA MAUDE (device adverse events)

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