Boston Scientific DGP-PMC2-25Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 15060441917642), received between May 2, 2023 and May 2, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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.

• InjuryMay 2, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

  ON 17TH APRIL 2023 THE UK FACILITY HAS RECEIVED A CUSTOMER COMPLAINT FROM THE CUSTOMER BOSTON SCIENTIFIC REGARDING: - IT WAS REPORTED THAT: GROUNDING PAD BURN, BURNED TWO PATIENTS ONE YESTERDAY, (B)(6) 2023 AND ONE TODAY, (B)(6) 2023, GROUNDING PADS USED NIKMED PAD BY BSC REFERENCE 2407 YESTERDAY, (B)(6) 2023 BSC NEUTURO NONWIRED. ADDITIONAL INFORMATION WAS RECEIVED THAT PATIENT WAS TREATED WITH BACITRACIN ANTIBIOTIC OINTMENT AND DRY BANDAGE. THIS RECORD IS FOR THE PATIENT BURNED ON (B)(6) 2023. NO LOT NUMBER PROVIDED. DUE TO MEDICAL INTERVENTION, NMT FINDS THIS EVENT TO BE REPORTABLE.

  Patient problems: Burn(s)

  MAUDE report 16855870 ↗