Medline Industries, Inc. DYND74285Recalls & reported problems
Medline Industries, Inc. · KIT,IV START · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10884389529188), received between Aug 17, 2023 and May 22, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (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
- Difficult or Delayed Positioning1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 22, 2026Difficult or Delayed Positioning
THE PAPER WILL NOT PEEL OFF THE TEGADERM DRESSING AND THE DRESSING PEELS UP FROM THE PATIENT'S SKIN, LEADING TO A IV OPEN TO AIR CREATING AN INFECTION CONTROL CONCERN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25260910 ↗MalfunctionSep 19, 2023
3M TEGADERM COULD NOT SEPERATE WITH EDGES FOR APPLICATION. COULD NOT BE USED. ADDITIONAL KIT REQUIRED. EQUIPMENT RETAINED IF DESIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17773649 ↗MalfunctionAug 21, 2023
3M TEGADERM WITHOUT WINDOW. COULD NOT BE USED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17583696 ↗MalfunctionAug 21, 2023
3M TEGADERM COULD NOT SEPARATE WITH EDGES FOR APPLICATION. COULD NOT BE USED. ADDITIONAL KIT REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17583691 ↗MalfunctionAug 21, 2023
IV START KIT MEDLINE REF DYND74285. 3M TEGADERM COULD NOT SEPARATE WITH EDGES FOR APPLICATION. COULD NOT BE USED. ADDITIONAL KIT REQUIRED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17583669 ↗MalfunctionAug 17, 2023
MEDLINE IV START KIT 3M TEGADERM FROM KIT DOES NOT HAVE WINDOW CUT. UNABLE TO BE USED. ADDITIONAL KIT OPENED. THIS HAD HAD MULTIPLE OCCURRENCES RECENTLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17563297 ↗
Other I.V. start kit devices
- Medline Industries, Inc. CDS860014PMedline Industries, Inc. · I.V. start kit3 recalls0 reports
- Medline Industries, Inc. DYKM1000BMedline Industries, Inc. · I.V. start kit3 recalls0 reports
- MEDLINE DYNJ68937AMedline Industries, Inc. · I.V. start kit2 recalls2 reports
- Centurion IVS3940BCenturion Medical Products Corporation · I.V. start kit2 recalls0 reports
- Centurion CVI3650Centurion Medical Products Corporation · I.V. start kit2 recalls0 reports
- MEDLINE DYNDV2465Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- MEDLINE PICC0010Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- Centurion IVS3900ACenturion Medical Products Corporation · I.V. start kit2 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 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