Artisan Power MB-8713030-NRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00819595015418), received between Mar 31, 2026 and Mar 31, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Difficult to Setup or Prepare” (1 report).

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

• MalfunctionMar 31, 2026Device Difficult to Setup or Prepare; Insufficient Flow or Under Infusion

  AS REPORTED BY THE USER FACILITY: WE HAVE SEEN A COUPLE SAFEDAY REPORTS RECENTLY ABOUT THERE BEING MORE VERSED LEFT IN THE SYRINGE THAN THERE SHOULD HAVE BEEN BASED ON CHARTING AND THE RATE OF INFUSION. VERSED COMES IN A MANUFACTURER SYRINGE THAT IS A BD 30ML SYRINGE. WHEN LOOKING AT THE PUMP LOGS, IT WOULD SHOW THAT THE NURSE CHOSE THE 50ML SYRINGE SIZE WHEN PROGRAMMING THE PUMP, CAUSING THE DISCREPANCY AND ULTIMATELY ALTERING DRUG DELIVERY. BUT WHEN YOU PLACE A 30ML SYRINGE IN THE PUMP, IT ONLY PROMPTS FOR 20ML OR 30ML.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24742980 ↗