IDEAL IMPLANT Structured Breast Implant, saline breast implant, in the following sizes recall — FDA Z-2219-2019
The implants were deflating due to a piece of silicone disrupting the seal of the posterior valve shortly after implantation.
Overview of recall records associated with Ideal Implant Inc., including dates, categories and classifications where available.
Classification mix: Class II: 1.
The implants were deflating due to a piece of silicone disrupting the seal of the posterior valve shortly after implantation.
This page summarizes recall records in which the official source identifies Ideal Implant Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.