MARQUEE MQ2016Recalls & reported problems
Bard Peripheral Vascular, Inc. · MARQUEE® Disposable Core Biopsy Instrument, 20g x 16cm · Class 2
All models of MARQUEE (26)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00801741097249), received between Oct 9, 2025 and Oct 9, 2025 — classified as 3 injuries.
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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Pneumothorax3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A LUNG BIOPSY USING THE MARQUEE. DURING THE PROCEDURE, PATIENT EXPERIENCING PNEUMOTHORAX. HOWEVER, THE CURRENT PATIENT STATUS UNKNOWN.
Patient problems: Pneumothorax
MAUDE report 23263147 ↗InjuryOct 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A LUNG BIOPSY USING THE MARQUEE. DURING THE PROCEDURE, PATIENT EXPERIENCING PNEUMOTHORAX. HOWEVER, THE CURRENT PATIENT STATUS UNKNOWN.
Patient problems: Pneumothorax
MAUDE report 23263142 ↗InjuryOct 9, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
ON (B)(6) 2025, A PATIENT UNDERWENT A LUNG BIOPSY USING THE MARQUEE. DURING THE PROCEDURE, PATIENT EXPERIENCING PNEUMOTHORAX. HOWEVER, THE CURRENT PATIENT STATUS UNKNOWN.
Patient problems: Pneumothorax
MAUDE report 23263141 ↗
Other INSTRUMENT, BIOPSY devices
- MAX-CORE MC1616Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall4,258 reports
- ENCOR® ECP017GSenorx, Inc. · INSTRUMENT, BIOPSY1 recall4,186 reports
- MAX-CORE MC1820Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall2,404 reports
- MAX-CORE MC1816Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall1 death848 reports
- MAX-CORE MC1410Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall399 reports
- MAX-CORE MC1610Bard Peripheral Vascular, Inc. · INSTRUMENT, BIOPSY1 recall394 reports
- ENCOR® ECP0110GVSenorx, Inc. · INSTRUMENT, BIOPSY392 reports
- ENCOR® ECP0110GSenorx, Inc. · INSTRUMENT, BIOPSY390 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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