Esteem Synergy Stomahesive Skin Barrier, part of Esteem synergy, which is a two-piece ostomy system consisting of an adhesive skin barrier and an adhesive pouch: ESTEEM SYN FLX WHT16/35MM PRECUT(1X10), REF: 405473; ESTEEM SYN FLX WHT35/35MM PRECUT(1X10), REF: 405479
FDA Recall Z-0903-2025 · Posted 2025-01-10
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Recalling FirmConvaTec, Inc
Recall StatusOpen, Classified
Product CodeEXE
Date Initiated2024-11-29
Product Quantity240
Reason for Recall
Ostomy skin barrier package contains a pre-cut wafer of 28mm instead of 16mm and/or 35mm
pre-cut wafers, as stated package labeling. If pre-cut wafers are too big the device cannot be used and if the pre-cut wafer is too small and the device user tries to apply, this could cause abrasion, stomal cut, and bleeding
Firm Action
On 11/29/2024, "URGENT: MEDICAL DEVICE RECALL" notices were emailed to customers who were asked to do the following:
1) Review this notification and ensure all relevant stakeholders are aware of this recall
communication and any action required.
2) If you have distributed affected product beyond your establishment, identify your customers, and notify them at once of this product recall. Your notification to your customers can be enhanced by including a copy of this recall notification letter.
3) Immediately examine your inventory and quarantine affected product
Upon receipt and review of satisfactory information, formal authorization from a firm
Representative will be provided to proceed with product destruction.
4) Firm will provide a Certificate of Destruction (COD) to complete.
5) Immediately destroy all affected product and provide firm with a signed Certificate of
Destruction (COD) as evidence to support reconciliation and regulatory reporting.
6) Complete and return the response form via email to [email protected]
9. Your account will be credited for destroyed product upon receipt of the response form and Certificate of Destruction (COD).
If you need any further information or support concerning this recall, please contact any of the following [email protected], [email protected] or telephone 800-582-6514.
Root Cause
Process control
Distribution Pattern
US distribution to states of: OH, NY, IL
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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