MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-03-31 for STYLE 68 SALINE FILLED BREAST IMPLANT 68HP-550 manufactured by Allergan (costa Rica).
[186199633]
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. Further information from the reporter regarding event, product, or patient details has been requested. No additional information is available at this time. The reason for reoperation is deflation.
Patient Sequence No: 1, Text Type: N, H10
[186199654]
Healthcare professional reported right side deflation. Device remains implanted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9617229-2020-05294 |
MDR Report Key | 9905449 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2020-03-31 |
Date of Report | 2020-03-31 |
Date of Event | 2020-02-27 |
Date Mfgr Received | 2020-03-03 |
Device Manufacturer Date | 2011-04-02 |
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 | STYLE 68 SALINE FILLED BREAST IMPLANT |
Generic Name | PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE |
Product Code | FWM |
Date Received | 2020-03-31 |
Catalog Number | 68HP-550 |
Lot Number | 2097210 |
Device Expiration Date | 2015-03-02 |
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 |