Medical Action Industries 81208Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10809160341797), received between Jun 6, 2023 and Jun 6, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Patient Device Interaction Problem” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 6, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  MAI COMPLAINT #: (B)(4). PATIENT ONE: PATIENTS IN THE ICU WERE EXPERIENCING REDNESS, BLISTERING, IRRITATION, ITCHY BURNING SENSATION AROUND THE TEGADERM ADHESIVE. A PATIENT WITH A DIALYSIS CATHETER (IJ) HAD A PICC DRESSING KIT THAT WAS USED ON (B)(6). A BLISTERING/SKIN TEAR WAS NOTICED ON (B)(6) 2023 AND THE PATIENT RECEIVED WOUND CARE TREATMENT ON (B)(6) 2023. THE PATIENT IS ALLERGIC TO ALEVE, NAPROXEN AND TUBERCULIN SKIN TEST.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 17076253 ↗
• InjuryJun 6, 2023Patient Device Interaction Problem; Patient Device Interaction Problem

  MAI COMPLAINT #: (B)(4). PATIENT TWO: A PATIENT WITH A CENTRAL LINE (IJ) THAT WAS INSERTED ON (B)(6) HAD A DRESSING CHANGE ON (B)(6) USING A PICC DRESSING KIT. THE BLISTERING AND ITCHINESS WAS REPORTED ON (B)(6) WHICH WAS ALSO OBSERVED BY THE NURSE. PATIENT HAD SKIN CLEANED AND MARATHON APPLIED FOR FUTURE DRESSINGS. THE PATIENT HAD NO KNOWN ALLERGIES.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 17076051 ↗