ReliaTect® Post-Op Dressing with CHG 0496-0568-76Recalls & reported problems
Avery Dennison Corporation · ReliaTect® Post-Op Dressing with CHG, Large, 3.9 x 9.8 in (10 x 25 cm) · Class U
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00817138010517), received between Jan 13, 2021 and Jan 13, 2021 — classified as 2 injuries.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Rash1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJan 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AVERY DENNISON RECEIVED A COMPLAINT FROM THE OB/GYN DEPARTMENT OF A HOSPITAL IN FLORIDA THROUGH ITS DISTRIBUTOR. THE COMPLAINT INDICATED THAT SKIN REDNESS WAS OBSERVED AFTER USE OF THE RELIATECT POST-OP DRESSING WITH CHG ON A PATIENT THAT UNDERWENT A C-SECTION SURGICAL PROCEDURE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11164625 ↗InjuryJan 13, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
AVERY DENNISON RECEIVED A COMPLAINT FROM THE OB/GYN DEPARTMENT OF A HOSPITAL IN (B)(6) THROUGH ITS DISTRIBUTOR. THE COMPLAINT INDICATED THAT A RASH WAS OBSERVED AFTER THE USE OF THE RELIATECT POST-OP DRESSING WITH CHG ON A PATIENT THAT UNDERWENT A C-SECTION SURGICAL PROCEDURE.
Patient problems: Rash
MAUDE report 11164618 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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