Ideal Implant recalls saline breast implants (210cc-675cc) due to silicone disrupting the posterior valve seal, causing deflation. Affected units have serial numbers 0100292-0102777.
The implants were deflating due to a piece of silicone disrupting the seal of the posterior valve shortly after implantation.
Ideal Implant is recalling saline breast implants in sizes 210cc to 675cc because a piece of silicone can disrupt the seal after implantation, leading to deflation. This could cause discomfort or complications if the implant loses pressure.
The implants can deflate because a piece of silicone disrupts the posterior valve seal shortly after implantation. This causes the implant to lose pressure, which may lead to discomfort or complications if the implant is no longer properly contained.
Women who received saline breast implants from Ideal Implant with serial numbers between 0100292 and 0102777 are affected. Those who have implants that have been in place for a while may be at higher risk of deflation.
Check if your implant has a serial number between 0100292 and 0102777. The product includes saline breast implants in sizes ranging from 210cc to 675cc.
Look for the serial number on your implant, which should be between 0100292 and 0102777.
The recall does not require immediate discontinuation; however, you should check if your implant is affected and contact Ideal Implant if you have concerns.
If your implant deflates, it may cause discomfort or complications, but the recall does not specify a specific action for deflated implants.
Check the serial number on your implant; if it falls between 0100292 and 0102777, it is affected.
We’ve drafted a message you can send Ideal Implant to request your refund or repair — edit it as you like.
Subject: Recall Z-2219-2019 — Ideal Implant Ideal Implant Hello, I own a Ideal Implant that is covered by recall Z-2219-2019 from Ideal Implant. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
