Medline MDSPHY200Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277635029), received between Aug 14, 2026 and Sep 16, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 16, 2026Patient Device Interaction Problem

  Patient problems: Burn(s)

  MAUDE report 50788073 ↗
• InjuryAug 14, 2026Improper or Incorrect Procedure or Method

  75 YOM BIB EMS from SNF obtunded/ unresponsive cardiac arrest PEA. Intubated went into V-FIB. Stryker LP35 connected to Medline pads. Shock x1 at 360 joules. Appears spark from pad occurred, flame from pathway from defib pad to chest hair. BVM on gurney on pathway. Burns to chest, neck, left arm, left flank with no specific burn treatment. Bag valve mask connected to oxygen near patient's left side. Patient skin was shaved prior to shock.

  Patient problems: Burn(s)

  MAUDE report 50255256 ↗