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MISSION 2010MSRecalls & reported problems

Bard Peripheral Vascular, Inc. · Mission Disposable Core Biopsy Instrument - 20Gx10cm · Class 2

All models of MISSION (20)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
3
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741097027), received between Nov 9, 2020 and Aug 7, 2023 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Device Contamination with Chemical or Other Material” (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 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Device Contamination with Chemical or Other Material1
  • Device Markings/Labelling Problem1
  • Difficult to Remove1
  • Failure to Fire1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Hematoma1
  • Hemoptysis1
  • Hemorrhage/Blood Loss/Bleeding1
  • Pain1

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 7, 2023Difficult to Remove; Failure to Fire; Device Contamination with Chemical or Other Material; Difficult to Remove; Failure to Fire; Device Contamination with Chemical or Other Material

    IT WAS REPORTED THAT DURING A BIOPSY PROCEDURE, THE RESISTANCE WAS ALLEGEDLY NOT SMOOTH WHEN THE NEEDLE WAS PULLED OUT. IT WAS FURTHER REPORTED THAT AFTER REMOVING THE NEEDLE, AN IRON WIRE WAS ALLEGEDLY FOUND INSIDE. THERE WAS NO REPORTED PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17468638 ↗
  • MalfunctionMar 23, 2022Device Markings/Labelling Problem; Device Markings/Labelling Problem

    IT WAS REPORTED THAT PRIOR TO A BIOPSY PROCEDURE, THE LABELS IN THE PRODUCT AND THE PACKAGE WERE ALLEGEDLY MISMATCHING. THERE WAS NO PATIENT CONTACT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13860685 ↗
  • InjuryNov 9, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THROUGH A (B)(6) CLINICAL FOLLOW-UP SURVEY ON CORE BIOPSY INSTRUMENTS, THERE WERE 2 OCCURRENCES OF HEMATOMA, 2 OCCURRENCES OF HEMORRHAGE, AND 2 OCCURRENCES OF PAIN DURING KIDNEY BIOPSY PROCEDURE(S). IT WAS FURTHER REPORTED THERE WAS 1 OCCURRENCE OF HEMOPTYSIS REQUIRING HOSPITALIZATION OR SPECIFIC THERAPY, 2 OCCURRENCES OF PAIN, AND 2 OCCURRENCES OF THORACOSTOMY TUBE PLACEMENT REQUIRING PROLONGED ADMISSION, CATHETER EXCHANGE OR PLEURODESIS DURING LUNG BIOPSY PROCEDURE(S). THERE CURRENT STATUS OF THE PATIENT(S) WAS NOT PROVIDED.

    Patient problems: Hematoma; Hemoptysis; Hemorrhage/Blood Loss/Bleeding; Pain

    MAUDE report 10808124 ↗

Other INSTRUMENT, BIOPSY devices

All INSTRUMENT, BIOPSY devices →

Sources and updates

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