ConvaTec recalls Esteem+ Drainable Pouch (REF 416975) due to impaired release liner functionality. This may affect stoma output management after colostomy or ileostomy procedures.
impaired functionality of the release liner
ConvaTec is recalling its Esteem+ Drainable Pouch product because the release liner may not function properly. This could lead to issues with managing stoma output after surgery. Affected users should check their product details and follow the official recall instructions.
The release liner in the pouch may not function properly, which could cause problems with removing the pouch from the stoma site. This might lead to improper stoma output management.
People who use ConvaTec Esteem+ Drainable Pouch for stoma output management after colostomy or ileostomy procedures are likely affected. Those with recent stoma surgery are at higher risk.
Check for the product name 'ConvaTec Esteem+ Drainable Pouch', size 3/4-2 1/4 in., and reference number REF 416975. The batch number is 2A02671 and UDI/DI is 768455115334.
Identify the product name, size, reference number, and batch number to confirm if it's affected.
The recall is due to impaired release liner functionality, which may affect stoma output management. However, the hazard is not described as causing serious injury, so it's considered low risk.
The recall does not specify a remedy, so check the product details and contact ConvaTec for further instructions.
Look for the product name 'ConvaTec Esteem+ Drainable Pouch', size 3/4-2 1/4 in., reference number REF 416975, batch number 2A02671, and UDI/DI 768455115334.
We’ve drafted a message you can send ConvaTec to request your refund or repair — edit it as you like.
Subject: Recall Z-0128-2023 — ConvaTec ConvaTec Hello, I own a ConvaTec that is covered by recall Z-0128-2023 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.
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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.
