MISSION 2020MSRecalls & reported problems
Bard Peripheral Vascular, Inc. · Mission Disposable Core Biopsy Instrument - 20Gx20cm · Class 2
Quick summary
This Bard Mission disposable biopsy instrument is used to take core tissue samples. The 24 reports describe incorrect or expired expiry dates noticed on the package before use, with no patient contact, and list no deaths and no injuries. No recalls name this device, with 0 reports in the recent period compared with 24 in the earlier period.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 24
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 00801741097041), received between Jul 22, 2025 and Jul 23, 2025 — classified as 24 malfunctions.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (24 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Markings/Labelling Problem24
Patient problems
- No Clinical Signs, Symptoms or Conditions24
Recent adverse event reports
The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION INSTRUMENT. PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE EXPIRED. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22575973 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION INSTRUMENT. PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE EXPIRED. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22575972 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION INSTRUMENT. PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE EXPIRED. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22574708 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION INSTRUMENT. PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE EXPIRED. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22574697 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT WAS GETTING PREPARED FOR A BIOPSY PROCEDURE USING MISSION DEVICE. IT WAS REPORTED THAT PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE INCORRECT. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22574215 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE USING MISSION DEVICE. IT WAS REPORTED THAT PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE INCORRECT. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22573765 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT WAS GETTING PREPARED FOR A BIOPSY PROCEDURE USING MISSION DEVICE. IT WAS REPORTED THAT PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE INCORRECT. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22573752 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT WAS PREPPED FOR A BIOPSY PROCEDURE USING MISSION DEVICE. IT WAS REPORTED THAT PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE INCORRECT. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22573696 ↗MalfunctionJul 23, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE USING MISSION DEVICE. IT WAS REPORTED THAT PRIOR TO THE PROCEDURE, THE EXPIRY DATE MENTIONED IN THE PACKAGE WAS FOUND TO BE INCORRECT. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22573692 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563149 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563105 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS ON (B)(6) 2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563103 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563029 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563026 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22563023 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562903 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562902 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562897 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562896 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562895 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562894 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562893 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS 18/4/2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS 28/5/2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562784 ↗MalfunctionJul 22, 2025Device Markings/Labelling Problem; Device Markings/Labelling Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A BIOPSY PROCEDURE WITH THE MISSION DEVICE. PRIOR TO THE PROCEDURE, A DISCREPANCY WAS NOTED BETWEEN THE DELIVERY NOTE AND LABEL IN THE PACKING. ON THE DELIVERY NOTE, THE STERILITY DATE IS (B)(6) 2027 AND ON THE LABEL OF THE ACTUAL PRODUCT IS (B)(6) 2025. THERE WAS NO PATIENT CONTACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22562780 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.