ConvaTec recalls Esteem+ Drainable Pouches with impaired release liner functionality. Affected units have specific UDI/DI and batch numbers for colostomy/ileostomy stoma management.
impaired functionality of the release liner
ConvaTec is recalling its Esteem+ Drainable Pouches due to a release liner that may not function properly. This could lead to improper stoma output management and potential discomfort or complications for users.
The release liner in these pouches may not function correctly, which could cause improper stoma output management. This might lead to discomfort or complications if the pouch does not seal properly or release stool effectively.
People who use ConvaTec Esteem+ Drainable Pouches for stoma output management after colostomy or ileostomy surgery are likely affected. Those with specific UDI/DI numbers and batch dates are at higher risk.
Check for the UDI/DI number 768455115358 and batch numbers 2A00585, 2A00586, 2A04528, 2A04529, or 2A04530m on the product packaging.
Look for the UDI/DI number 768455115358 and batch numbers 2A00585, 2A00586, 2A04528, 2A04529, or 2A04530m on the pouch packaging.
The release liner may not function properly, which could lead to improper stoma output management.
Check for the UDI/DI number 768455115358 and batch numbers 2A00585, 2A00586, 2A04528, 2A04529, or 2A04530m on the packaging.
The recall does not specify a stop-use instruction, so you can continue using them if they are functioning properly.
We’ve drafted a message you can send ConvaTec to request your refund or repair — edit it as you like.
Subject: Recall Z-0127-2023 — ConvaTec ConvaTec Hello, I own a ConvaTec that is covered by recall Z-0127-2023 from ConvaTec. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
