Medline MDSB10700Recalls & reported problems
Medline Industries, Inc. · SCANNER,BLADDER,BIOCON 700,W/PRINTER · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 40884389154893), received between Sep 17, 2026 and Sep 30, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Material Frayed” (3 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. 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
- Material Frayed3
- Break2
- Battery Problem1
- Calibration Problem1
- Connection Problem1
- Fluid/Blood Leak1
- Inadequate Lubrication1
- Incorrect, Inadequate or Imprecise Result or Readings1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Battery Problem
It was reported that PRODUCT SCREEN COMES UP WITH ERROR CODE E005 BATTERY ERROR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50944590 ↗MalfunctionSep 24, 2026Break; Material Frayed; Inadequate Lubrication
It was reported that "THE PROBE IS SHATTERED AND NEEDS OIL, POWER CORD IS FRAYED."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50883746 ↗MalfunctionSep 23, 2026No Visual Prompts/Feedback
It was reported that "SCANNER IS NOT SHOWING PINK CROSS HAIRS WHEN TRYING TO SCAN."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50867891 ↗MalfunctionSep 23, 2026Incorrect, Inadequate or Imprecise Result or Readings; Calibration Problem
It was reported that "It read incorrectly 0ml patient had 500ml" and the customer was "Having accuracy reading issues as well as issues passing the cal kit" and "Getting the error messages "ec10, ec15."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50866679 ↗MalfunctionSep 22, 2026Connection Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50861304 ↗MalfunctionSep 22, 2026Break; Material Frayed
It was reported that the wire that is connected to the probe is frayed and broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853105 ↗MalfunctionSep 18, 2026Low Readings
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50822708 ↗MalfunctionSep 17, 2026Fluid/Blood Leak; Material Frayed
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50809780 ↗
Other System, imaging, pulsed echo, ultrasonic devices
- EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE OLYMPUS GF TYPE UCT180Olympus Medical Systems Corp. · System, imaging, pulsed echo, ultrasonic1 recall8 deaths5,133 reports
- Site~Rite 8 Ultrasound System 9770600Bard Access Systems, Inc. · System, imaging, pulsed echo, ultrasonic629 reports
- Site-Rite 9770501Bard Access Systems, Inc. · System, imaging, pulsed echo, ultrasonic546 reports
- Transducer X8-2t 989605455171Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic8 recalls19 reports
- Transducer C10-3v 989605409562Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic7 recalls0 reports
- Site~Rite 8 Ultrasound System 9770600YBard Access Systems, Inc. · System, imaging, pulsed echo, ultrasonic330 reports
- Transducer C9-2 989605391092Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 reports
- Transducer S5-1 989605412082Philips Ultrasound LLC · System, imaging, pulsed echo, ultrasonic5 recalls0 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.
How reports and recalls are matched · Editorial policy · Report an error on this page