Medline Industries, Inc. DYND74260Recalls & reported problems
Medline Industries, Inc. · IV START KIT W/CHLORAPREP APP · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 14
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 14 adverse event reports that list this exact device (DI 10080196992980), received between Sep 22, 2026 and Sep 30, 2026 — classified as 14 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (8 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
- Loss of or Failure to Bond8
- Physical Resistance/Sticking4
- Adhesive Too Strong2
- Unsealed Device Packaging1
Patient problems
- No Clinical Signs, Symptoms or Conditions14
Recent adverse event reports
The 14 most recent of 14 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Physical Resistance/Sticking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952546 ↗MalfunctionSep 30, 2026Loss of or Failure to Bond
It was reported that "having quality concerns regarding the backing on our suresite dressing in a stocked kit."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952439 ↗MalfunctionSep 30, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50952414 ↗MalfunctionSep 29, 2026Loss of or Failure to Bond
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50938265 ↗MalfunctionSep 28, 2026Unsealed Device Packaging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918152 ↗MalfunctionSep 25, 2026Loss of or Failure to Bond
It was reported that "The film is difficult to take off with the tabs. The film is staying on the backing and not able to be peeled off correctly."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50899162 ↗MalfunctionSep 25, 2026Loss of or Failure to Bond
It was reported that "suresite dressing is failing in almost every way."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50896764 ↗MalfunctionSep 25, 2026Adhesive Too Strong
It was reported that the back of the Tegaderms are not peeling off making them unusable.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50896047 ↗MalfunctionSep 23, 2026Loss of or Failure to Bond
It was reported that WHEN THEY PEEL BACK THE TEGADERM THE ADHESIVE SIDE IS NOT STICKY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870248 ↗MalfunctionSep 23, 2026Loss of or Failure to Bond
It was reported that "Transparent film dressing not coming off plastic backing when peeling off."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50866896 ↗MalfunctionSep 22, 2026Physical Resistance/Sticking
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50861448 ↗MalfunctionSep 22, 2026Physical Resistance/Sticking
It was reported that "Several of the dressing that comes in the pack is defective" and "It does not peel off the paper and can not be placed over the IV site."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50857244 ↗MalfunctionSep 22, 2026Adhesive Too Strong
It was reported that the dressing that is included in the kit was used in or and was not pulling apart properly. Adhesive plastic is not separating.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50854785 ↗MalfunctionSep 22, 2026Loss of or Failure to Bond; Physical Resistance/Sticking
It was reported that "Defective tagaderm, will not come off the adhesive, not usable."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50853816 ↗
Other I.V. start kit devices
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- 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.
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