MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2020-03-31 for INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT N-TSF415 manufactured by Allergan (costa Rica).
[186282910]
A review of the device history record has been initiated. If any new, changed or corrected information is noted, a supplemental medwatch will be submitted. Reason for reoperation: rupture.
Patient Sequence No: 1, Text Type: N, H10
[186282911]
Healthcare professional reported left side rupture,strong pain and capsular contracture grade i. The device has been explanted with non allergan device.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9617229-2020-05280 |
MDR Report Key | 9908064 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-02-25 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2013-12-20 |
Date Added to Maude | 2020-03-31 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MRS. MICHELLE BURGESS |
Manufacturer Street | 12331-A RIATA TRACE PARKWAY BUILDING 3 |
Manufacturer City | AUSTIN TX 78727 |
Manufacturer Country | US |
Manufacturer Postal | 78727 |
Manufacturer Phone | 7372473605 |
Manufacturer G1 | ALLERGAN (COSTA RICA) |
Manufacturer Street | 900 PARKWAY GLOBAL PARK ZONA FRANCA |
Manufacturer Country | CS |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT |
Generic Name | PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED |
Product Code | FTR |
Date Received | 2020-03-31 |
Catalog Number | N-TSF415 |
Lot Number | 2539701 |
Device Expiration Date | 2018-12-20 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALLERGAN (COSTA RICA) |
Manufacturer Address | 900 PARKWAY GLOBAL PARK ZONA FRANCA CS |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-31 |