Coloplast recalls Titan Touch Scro Zero Ang 20cm inflatable penile prostheses with potential premature pump failure due to wall thickness issues. Affected units have specific catalog and lot numbers.
A decrease in wall thickness has the potential for a premature pump failure, compared to a pump with standard wall thickness, based on the number of interactions with the pump to inflate and deflate the penile prosthesis.
Coloplast is recalling certain Titan Touch Scro Zero Ang 20cm inflatable penile prostheses because a decrease in wall thickness may cause premature pump failure. This could lead to the device not functioning properly during use.
The pump in these prostheses has thinner walls than standard, which may lead to it failing earlier than expected when inflating or deflating the device. This could cause the prosthesis to stop working before the intended use period.
Men who own or use the recalled Titan Touch Scro Zero Ang 20cm inflatable penile prosthesis with catalog number ES29202400 and specific lot numbers (8904188, 8806754, 8806755) are affected. These individuals are at risk of the pump failing prematurely.
Check for the catalog number ES29202400 on the product. The affected units have specific lot numbers: 8904188, 8806754, or 8806755.
Look for the catalog number ES29202400 and lot numbers 8904188, 8806754, or 8806755 on the device.
The recalled product is the Titan Touch Scro Zero Ang 20cm inflatable penile prosthesis with catalog number ES29202400.
Lot numbers 8904188, 8806754, and 8806755 are affected.
The recall record does not specify a remedy.
We’ve drafted a message you can send Coloplast to request your refund or repair — edit it as you like.
Subject: Recall Z-1370-2023 — Coloplast Coloplast Hello, I own a Coloplast that is covered by recall Z-1370-2023 from Coloplast. 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.
