HydroMID MID-251Recalls & reported problems
Access Vascular, Inc. · HydroMID 5Fr Dual Lumen Marked catheter · Class 2 · Implant
- 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 00850030354426), received between Sep 17, 2025 and Sep 17, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 17, 2025Fluid/Blood Leak; Fluid/Blood Leak
COMPANY REPRESENTATIVE WAS CONTACTED BY A CUSTOMER TO STATE THAT AN INSERTED CATHETER WAS LEAKING INFUSATE. THE CUSTOMER REPORTED THAT THE CATHETER WAS INSERTED A MONTH AGO. THE FLOOR STAFF CALLED THE IV TEAM BECAUSE THE CATHETER WAS NOT FLUSHING AND LEAKING AT THE SITE AS WELL AS SWELLING NEAR THE INSERTION SITE AND NOT FLUSHING. INITIALLY HE FELT THAT THE LINE MAY HAVE BEEN DAMAGED BY STAFF ON DRESSING CHANGE. A VIDEO TAKEN BY THE CUSTOMER SHOWED A LEAK AT THE 0 CM MARK. THE CUSTOMER REPORTED THAT THE CATHETER WAS DISCARDED UPON REMOVAL. .
Patient problems: Insufficient Information
MAUDE report 23077796 ↗
Other Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days devices
- BD Insyte Autoguard 382523Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days660 reports
- BD Insyte Autoguard 382533Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls527 reports
- BD PosiFlush 306546Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 death608 reports
- BD Insyte Autoguard Shielded IV Catheter 381823Becton, Dickinson And Company · Catheter, intravascular, therapeutic, short-term less than 30 days582 reports
- BD Insyte Autoguard 381423Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall528 reports
- BD Insyte Autoguard 382544Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall437 reports
- BD Nexiva, BD Q-Syte 383536Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls374 reports
- BD PosiFlush 306547Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days2 recalls1 death331 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.