Medline MDS9913HPRecalls & reported problems
Medline Industries, Inc. · CUFF,BP,DISP,1 TUBE,ADULT,HP · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10888277194854), received between Dec 28, 2023 and Sep 29, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Gas/Air Leak” (2 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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Gas/Air Leak2
- Device Sensing Problem1
- Inflation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 29, 2026Gas/Air Leak
It was reported that "item leaking when it pumps."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50931506 ↗MalfunctionSep 18, 2026Inflation Problem; Gas/Air Leak
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50821367 ↗MalfunctionDec 28, 2023Device Sensing Problem; Device Sensing Problem
BLOOD PRESSURE CUFF REQUIRED MULTIPLE RE-CYCLES
Patient problems: Insufficient Information
MAUDE report 18410856 ↗
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- DRIVEMEDICAL RTLFW19RW-RDDrive Devilbiss Healthcare · AID, TRANSFER2 reports
- VIVE LVA1028LVive Health LLC · Aid, Transfer1 report
- Drive RTL13083Drive Devilbiss Healthcare · AID, TRANSFER1 report
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.
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