MISSION 1810MSRecalls & reported problems

Summary

The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00801741096983), received between Oct 17, 2023 and Feb 24, 2026 — classified as 8 malfunctions.

The most frequently reported specific device problem is “Difficult to Remove” (5 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 8 most recent of 8 reports, in the reporter's own words as published by the FDA.

• MalfunctionFeb 24, 2026Self-Activation or Keying

  ON (B)(6) 2026, A PATIENT UNDERWENT AN ULTRASOUND GUIDED KIDNEY BIOPSY PROCEDURE THROUGH NORMAL DENSITY TISSUE USING A MISSION INSTRUMENT. AFTER FIRING THE DEVICE, AN ISSUE OCCURRED WITH THE INSTRUMENTS LOCKING SYSTEM FOLLOWING PUSHING THE INNER NEEDLE TO RETRIEVE THE SPECIMEN. SLIGHT NEEDLE MOVEMENT OCCURRED CRUSHING THE SPECIMEN. IT WAS FURTHER REPORTED THAT, WITHOUT PRESSING THE TRIGGER BUTTON, THE OUTER CANNULA RELEASED FROM THE PRIME POSITION. THE PROCEDURE WAS COMPLETED BY ANOTHER DEVICE. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24427087 ↗
• MalfunctionSep 29, 2025Difficult to Remove; Material Twisted/Bent; Difficult to Remove; Material Twisted/Bent

  ON (B)(6) 2025, A PATIENT UNDERWENT AN ULTRASOUND GUIDED LYMPHATIC BIOPSY THROUGH NORMAL DENSITY TISSUE USING THE MISSION. DURING THE PROCEDURE, THE DEVICE NEEDLE WAS FOUND TO BE BENT. FURTHERMORE, IT WAS REPORTED THAT IT IS DIFFICULT TO REMOVE FROM A PATIENT. NO COAXIAL NEEDLE WAS USED, AND THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. THERE WERE NO REPORTED PATIENT INJURIES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23165330 ↗
• MalfunctionSep 29, 2025Difficult to Remove; Material Twisted/Bent; Difficult to Remove; Material Twisted/Bent

  ON (B)(6) 2025, A PATIENT UNDERWENT AN ULTRASOUND GUIDED LYMPHATIC BIOPSY THROUGH NORMAL DENSITY TISSUE USING THE MISSION. DURING THE PROCEDURE, THE DEVICE NEEDLE WAS FOUND TO BE BENT. FURTHERMORE, IT WAS REPORTED THAT IT IS DIFFICULT TO REMOVE FROM A PATIENT. NO COAXIAL NEEDLE WAS USED, AND THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. THERE WERE NO REPORTED PATIENT INJURIES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23165328 ↗
• MalfunctionSep 29, 2025Difficult to Remove; Material Twisted/Bent; Difficult to Remove; Material Twisted/Bent

  ON (B)(6) 2025, A PATIENT UNDERWENT AN ULTRASOUND GUIDE LYMPHATIC BIOPSY PROCEDURE VIA NORMAL DENSITY TISSUE USING THE MISSION. DURING THE PROCEDURE, THE DEVICE NEEDLE WAS FOUND TO BE BENT. FURTHER IT WAS REPORTED THAT DIFFICULT TO REMOVE FROM PATIENT. NO COAXIAL NEEDLE WAS USED. THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23165052 ↗
• MalfunctionJul 29, 2025Difficult to Remove; Material Twisted/Bent; Difficult to Remove; Material Twisted/Bent

  ON (B)(6) 2025 A PATIENT UNDERWENT AN ULTRASOUND GUIDED BREAST BIOPSY THROUGH HARD DENSITY TISSUE USING MISSION KIT. DURING THE PROCEDURE, THE NEEDLE WAS BENT AND DIFFICULT TO REMOVE FROM THE PATIENT. THE PROCEDURE WAS COMPLETED BY ANOTHER DEVICE. THERE WAS NO PATIENT REPORTED INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22640141 ↗
• MalfunctionJul 29, 2025Difficult to Remove; Material Twisted/Bent; Difficult to Remove; Material Twisted/Bent

  (B)(6) 2025 A PATIENT UNDERWENT AN ULTRASOUND GUIDED BREAST BIOPSY THROUGH HARD DENSITY TISSUE USING MISSION KIT. DURING THE PROCEDURE, THE NEEDLE WAS BENT AND DIFFICULT TO REMOVE FROM THE PATIENT. THE PROCEDURE WAS COMPLETED BY ANOTHER DEVICE. THERE WAS NO PATIENT REPORTED INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22640133 ↗
• MalfunctionAug 27, 2024Break; Device Contamination with Chemical or Other Material; Break; Device Contamination with Chemical or Other Material

  IT WAS REPORTED THAT DURING A BIOPSY PROCEDURE, A PLASTIC ALLEGEDLY COMES OUT FROM THE INSIDE OF THE PRODUCT. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20075251 ↗
• MalfunctionOct 17, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT DURING A BIOPSY PROCEDURE, THE DEVICE SPRING ALLEGEDLY CAME OUT WHILE PRIMING. THE PROCEDURE WAS COMPLETED WITH ANOTHER DEVICE. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17947682 ↗