NEW IMAGE
Received Apr 15, 2026 · Event occurred Apr 6, 2026
Report 1119193-2026-00036 · MDR key 24891390
Device
Generic name
2-piece Ostomy Skin Barrier, Soft Convex, Ceraplus
Manufacturer
Hollister IncorporatedModel number
11704Catalog number
11704
Lot number
5J212
Product problems
- Adverse Event Without Identified Device or Use Problem
Patient
53 YR · Male
- Erythema
- Rash
- Urticaria
- Skin Inflammation/ Irritation
Narrative
Description of Event or Problem
IT WAS REPORTED THAT AN OSTOMATE EXPERIENCED SKIN IRRITATION, REDNESS AND OOZING UNDER THE BARRIER AFTER USING THREE DIFFERENT HOLLISTER PRODUCTS FOR A PERIOD OF TIME. THIS IS THE FIRST OF THE 3 PRODUCTS, 11704 HOLLISTER NEW IMAGE BARRIER. IT WAS REPORTED THAT THE PATIENT TRIED USING OTHER OSTOMY PRODUCTS AND THE IRRITATION BECAME WORSE. THE PATIENT REPORTED EVENTUALLY EXPERIENCING EXTREME ITCHINESS ON HIS ARMS, LEGS, CHEST AND BACK, WITH LITTLE BUMPS. THE PATIENT ALSO REPORTED HE WENT TO THE WOUND CARE NURSE AND WAS PRESCRIBED TRIAMCINOLONE CREAM AND A DIFFERENT BARRIER PRODUCT. IT WAS FURTHER REPORTED THAT THE REACTION CONTINUED AND THEN HE DEVELOPED A GENERALIZED REACTION WITH HIVES AND ITCHING OVER MOST OF HIS BODY. THE PATIENT REPORTED HE WENT TO THE URGENT CARE CENTER AND RECEIVED A STEROID SHOT AND A STEROID DOSE PACK AFTER WHICH HE FELT BETTER. HOLLISTER HAS ADVISED THE PATIENT TO SEEK ATTENTION FROM HIS HEALTH CARE PROFESSIONALS BEFORE USING THE HOLLISTER BARRIER AGAIN.
Additional Manufacturer Narrative
THE DEVICE WAS NOT RETURNED FOR ANALYSIS. DEVICE HISTORY REVIEW WAS CONDUCTED AND FOUND TO BE COMPLETE AND ACCURATE. IN VIVO SKIN SENSITIZATION TESTING IS PERFORMED TO IDENTIFY THE POTENTIAL RISK OF AN ALLERGIC RESPONSE. SOME INDIVIDUALS MAY STILL BE SENSITIVE TO A SPECIFIC MATERIAL THAT HAS MET ALL SENSITIZATION TEST REQUIREMENTS, AND THE SEVERITY OF THE REACTION CANNOT BE PREDICTED.