inforMED
InjuryFWM

UNK Mammary Implant

Received Jul 27, 2026

Report 9617229-2026-14155 · MDR key 50038812

Device

Generic name

Prosthesis, Breast, Inflatable, Internal, Saline

Catalog number

UNK Mammary Implant

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

Not reported

  • Wound Dehiscence

Narrative

Description of Event or Problem

Healthcare professional reported "Dehiscence". This record is for the left side. Device was explanted.

Additional Manufacturer Narrative

The event of Dehiscence is a physiological complication and analysis of the device generally does not assist Allergan in determining a probable cause for this event.Further information from the reporter regarding event, product, or patient details has been requested. No additional information is available at this time.Reason for Reoperation: Dehiscence.