Up&Up 245070726Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00017276226355), received between Jan 7, 2026 and Sep 16, 2026 — classified as 3 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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 50794152 ↗
• InjuryJun 4, 2026Adverse Event Without Identified Device or Use Problem

  IN THE INITIAL REPORT RECEIVED ON (B)(6) 2026, THE CONSUMER STATED THAT THE PRODUCT LEFT A RED MARK AND CAUSED A BURN. ACCORDING TO THE COMPLETED CONSUMER INFORMATION REPORT (CIR) RECEIVED ON (B)(6) 2026, THE CONSUMER CLARIFIED THAT SHE USED THE PRODUCT POST-SURGERY. SHE REPORTED THAT THE ADHESIVE BURNED HER SKIN. CONSUMER RETURNED THE PRODUCT TO THE STORE. THE CONSUMER RETURNED THE PRODUCT TO THE STORE AND HAD THE AFFECTED AREA EXAMINED BY HER DOCTOR, WHO CONFIRMED THE REACTION APPEARED TO BE CAUSED BY THE ADHESIVE. THE CONSUMER STATED THAT THE ISSUE WAS WITH THE TAPE AREA AND THAT SYMPTOMS RESOLVED AFTER SHE DISCONTINUED USING THE PRODUCT. HOWEVER, SHE STATED THAT SHE STILL HAS SCARRING.

  Patient problems: Burning Sensation; Skin Inflammation/ Irritation

  MAUDE report 25394868 ↗
• InjuryJan 7, 2026Adverse Event Without Identified Device or Use Problem

  IN THE INITIAL REPORT RECEIVED ON DECEMBER 12, 2025, THE CONSUMER STATED THAT WHEN SHE ATTEMPTED TO REMOVE THE BANDAGE, THE ADHESIVE CAUSED SKIN TEARING ON HER ABDOMEN. THIS RESULTED IN AN OPEN WOUND AND SCARRING. THE CONSUMER HAS BEEN TREATING THE AFFECTED AREA AT HOME AND WILL SEEK MEDICAL ATTENTION FOR POTENTIAL INFECTION. ON THE COMPLETED CONSUMER INFORMATION REPORT (CIR) RECEIVED ON DECEMBER 29, 2025, THE CONSUMER STATED THAT HER SKIN EXPERIENCED BLISTERING, BURNING, AND TEARING. PER THE CIR, THE CONSUMER STATED THAT THE ISSUE WAS WITH THE TAPE AREA. THE CONSUMER REQUIRED MEDICAL TREATMENT. THE DOCTOR AT URGENT CARE INFORMED THE CONSUMER THAT THE SYMPTOMS WERE CONSISTENT WITH CONTACT DERMATITIS. THE DOCTOR ADVISED THE CONSUMER THAT NO OTHER TREATMENT WAS AVAILABLE AT THE TIME. THE CONSUMER INFORMED THAT THE AREA IS IN THE STAGES OF HEALING AND HAS BEEN APPLYING NEOSPORIN AND HYDROCORTISONE CREAM. CONSUMER INFORMED THAT SYMPTOMS DID NOT CORRECT AFTER SHE STOPPED USING THE PRODUCT.

  Patient problems: Blister; Skin Inflammation/ Irritation

  MAUDE report 23989435 ↗