3M™ Micropore™ 1532-2Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 30707387763153), received between Dec 3, 2018 and Dec 3, 2018 — classified as 1 injury.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 3, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AN OUTPATIENT DIALYSIS FACILITY REPORTED THE FOLLOWING INFORMATION VIA A MEDWATCH FORM. APPROXIMATELY 45 MINUTES INTO A SCHEDULED 4 HOURS HEMODIALYSIS TREATMENT, THE MACHINE ALARMED ARTERIAL PRESSURE. STAFF FOUND PATIENT WITH VENOUS FISTULA NEEDLE DISLODGED, WITH TAPE INTACT ON WINGS OF THE FISTULA NEEDLE. A POOL OF BLOOD WAS NOTED BELOW THE CHAIR, WHICH CONTINUED TO THE WALL BEHIND THE CHAIR. CHAIR WAS IN SEMI-RECLINED POSITION. EBL 300 ML. PATIENT WAS UNRESPONSIVE WITH ERRATIC RESPIRATORY RATE. BLOOD PRESSURE WAS 112/60, PULSE 60. NORMAL SALINE WAS ADMINISTERED THROUGH THE ARTERIAL NEEDLE (TOTAL GIVEN 2.0L). PATIENT WAS PLACED IN TRENDELENBURG POSITION AND OXYGEN 10 L APPLIED VIA NASAL CANNULA. PATIENT WAS DROWSY BUT RESPONDING TO VERBAL STIMULI. EMS WAS CALLED, AND PATIENT WAS DISCHARGED WITH BLOOD PRESSURE 117/59, PULSE 62, RESP 18. ONE UNIT OF PRBC WAS ADMINISTERED IN THE ER AND PATIENT WAS THEN DISCHARGED HOME. PATIENT RETURNED TO THE FACILITY FOR HIS NEXT SCHEDULED HEMODIALYSIS TREATMENT ON (B)(6) 2018.

  Patient problems: Blood Loss; Hypovolemia; Loss of consciousness

  MAUDE report 8123840 ↗