Co-Axial Introducer Needle MCXS1810BPRecalls & reported problems
Argon Medical Devices, Inc. · Co-Axial Introducer Needle 17ga x 6.8cm · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00886333002443), received between Feb 27, 2024 and Feb 27, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Physical Resistance/Sticking” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Physical Resistance/Sticking1
Patient problems
- Needle Stick/Puncture1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 27, 2024Physical Resistance/Sticking; Physical Resistance/Sticking
A REPORT WAS RECEIVED VIA MEDSUN (B)(4) INDICATING PER DOCTOR'S NOTES, AN 18 G BIOPSY NEEDLE BECAME "STUCK" OR LODGED WITHIN A 17 G INTRODUCER NEEDLE DURING A BIOPSY OF AN ABDOMINAL MASS. BOTH OF THE NEEDLES WERE REMOVED FROM THE PATIENT AND WITH SOME EFFORT THE 18 G NEEDLE WAS PULLED FROM THE INTRODUCER NEEDLE. THE PURPOSE OF SEPARATING THE NEEDLES WAS TO RECOVER THE BIOPSY SPECIMEN. DURING SEPARATION OF THE NEEDLES, THE BIOPSY NEEDLE PUNCTURED THE SKIN OF THE ANTERIOR AND DISTAL LEFT INDEX FINGER OF DOCTOR. THE PUNCTURE SITE WAS CLEANED WITH ALCOHOL AND A BANDAGE APPLIED. IN A FOLLOW UP, IT WAS REPORTED THERE WERE NO LONG TERM INJURIES OR ADDITIONAL TREATMENT REQUIRED AND THE FINGER HEALED.
Patient problems: Needle Stick/Puncture
MAUDE report 18789150 ↗
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page