Plum 1239125Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI M3351239104251), received between Sep 21, 2018 and Jan 7, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Circuit Failure” (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 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.

• MalfunctionJan 7, 2026Excess Flow or Over-Infusion

  A REPORTED INCIDENT INVOLVING A PLUM A+ INFUSION PUMP CONCERNED A 75-YEAR-OLD PATIENT WITH A MEDICAL HISTORY OF DIABETES MELLITUS (DM), CHRONIC KIDNEY DISEASE (CKD), HYPERTENSION (HTN), DYSLIPIDEMIA (DLP), AND END-STAGE RENAL DISEASE (ESRD). THE PATIENT HAD BEEN ADMITTED WITH ACUTE CORONARY SYNDROME (ACS) PRESENTING A HIGH-RISK PATTERN AND UNDERWENT PERCUTANEOUS TRANSLUMINAL CORONARY ANGIOPLASTY (PTCA) WITH A DRUG-ELUTING STENT PLACED IN THE ANTERIOR DESCENDING ARTERY ON (B)(6) 2025. THE PATIENT ALSO HAD SEVERE SYMPTOMATIC AORTIC STENOSIS, FOR WHICH TRANSCATHETER AORTIC VALVE IMPLANTATION (TAVI) WAS PERFORMED ON (B)(6) 2025, FOLLOWED BY ENDARTERECTOMY FOR ACUTE POST-SURGICAL ISCHEMIA ON (B)(6) 2025. ADDITIONAL VASCULAR FINDINGS INCLUDED OCCLUSIONS OF THE SUPERFICIAL FEMORAL, POPLITEAL, AND PERONEAL ARTERIES ON THE RIGHT SIDE. ON (B)(6) 2025, THE PATIENT WAS PRESCRIBED ANTICOAGULATION THERAPY VIA A HEPARIN INFUSION PUMP AT A RATE OF 1050 IU PER HOUR. A NIGHT SHIFT NURSE REPORTED PREPARING A SOLUTION OF 25,000 IU OF HEPARIN IN 250 ML OF 0.9% SALINE AND PROGRAMMING THE PUMP ACCORDINGLY AT 8:50 PM, STATING THAT PHOTOS DOCUMENTING THE SETUP WERE SHARED WITH THE DAY SHIFT TEAM. AROUND NO

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24000176 ↗
• MalfunctionSep 21, 2018Circuit Failure; Circuit Failure

  CUSTOMER REPORTED THAT THE DEVICE USER (NURSE) RECEIVED AN ELECTRIC SHOCK BUT THERE WAS NO ADVERSE EVENT. THE CUSTOMER ALSO REPORTED THAT THE CORD WAS DAMAGED BUT THERE WERE NO EXPOSED WIRES. TESTING AND INVESTIGATION CONFIRMED THE DAMAGED AC POWER CORD. THE POWER CORD WAS REPLACED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7898127 ↗
• MalfunctionSep 21, 2018Circuit Failure; Circuit Failure

  CUSTOMER REPORTED THAT THE USER OF THE DEVICE (NURSE) RECEIVED AN ELECTRIC SHOCK AND THAT THE CABLE IS DAMAGED. AFTER DUE DILIGENCE NO ADDITIONAL INFORMATION RECEIVED. TESTING AND INVESTIGATION CONFIRMED THE DAMAGED AC POWER CORD. THE POWER CORD WAS REPLACED.

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 7898094 ↗