MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-03-11 for STYLE 410 FX RE-STERILIZABLE SIZER MSZFX775 manufactured by Allergan (costa Rica).
[138382829]
A review of the device history record has been completed. No deviations or non-conformances noted. Further information from the reporter regarding event, product, or patient details has been requested. No additional information is available at this time. This is a known potential adverse event addressed in the product labeling.
Patient Sequence No: 1, Text Type: N, H10
[138382830]
Healthcare provider reported left side? Doctor left sizers in a patient thinking they were implants.? Device has been explanted.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9617229-2019-01608 |
MDR Report Key | 8407958 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-03-11 |
Date of Report | 2019-03-11 |
Date Mfgr Received | 2019-02-15 |
Device Manufacturer Date | 2015-10-28 |
Date Added to Maude | 2019-03-11 |
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 | MS. SUZANNE WOJCIK |
Manufacturer Street | 301 W HOWARD LANE SUITE 100 |
Manufacturer City | AUSTIN TX 78753 |
Manufacturer Country | US |
Manufacturer Postal | 78753 |
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 410 FX RE-STERILIZABLE SIZER |
Generic Name | SIZER, MAMMARY, BREAST IMPLANT VOLUME |
Product Code | MRD |
Date Received | 2019-03-11 |
Catalog Number | MSZFX775 |
Lot Number | 2823883 |
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 | 2019-03-11 |