TAKE-APART 26184HVSRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04048551103098), received between Jun 12, 2025 and Jun 12, 2025 — classified as 2 injuries.

The most frequently reported specific device problem is “Activation 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJun 12, 2025Appropriate Device Problem Term/Code Not Available; Activation Failure; Appropriate Device Problem Term/Code Not Available; Activation Failure

  IT WAS REPORTED THAT DURING A LAPAROSCOPIC SPAY IN A CANINE PATIENT THE BIPOLAR SET WAS NOT WORKING. THE CAUTERIZATION DID NOT WORK. THE PRODUCT WAS STRIPPED DOWN AND THE INSERT TAKEN OUT. A BRAND-NEW INSERT AND NEW WIRE WAS USED AND STILL IT DID NOT WORK. IN THE END THE PROCEDURE WAS REVERTED TO PLACING A BIGGER PORT IN AND USING THE VET SEAL. THIS WORKED FINE. THE SURGERY WAS PROLONGED FOR MORE THAN 60 MINUTES. THE PATIENT HAD A SLOW RECOVERY DUE TO PROLONGED ANESTHETICS. CROSS REFERENCE MDR: 9610617-2025-00999, 9610617-2025-01015.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22198494 ↗
• InjuryJun 12, 2025Activation Failure; Activation Failure

  IT WAS REPORTED THAT DURING A LAPAROSCOPIC SPAY IN A CANINE PATIENT THE BIPOLAR SET WAS NOT WORKING. THE CAUTERIZATION DID NOT WORK. THE PRODUCT WAS STRIPPED DOWN AND THE INSERT TAKEN OUT. A BRAND-NEW INSERT AND NEW WIRE WAS USED AND STILL IT DID NOT WORK. IN THE END THE PROCEDURE WAS REVERTED TO PLACING A BIGGER PORT IN AND USING THE VET SEAL. THIS WORKED FINE. THE SURGERY WAS PROLONGED FOR MORE THAN 60 MINUTES. THE PATIENT HAD A SLOW RECOVERY DUE TO PROLONGED ANESTHETICS. CROSS REFERENCE MDR: 9610617-2025-00999; 9610617-2025-01015.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22198356 ↗