MEDLINE DYNDV2376ARecalls & reported problems
Medline Industries, Inc. · HOUSE WIDE IV START KIT · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10653160354451), received between Sep 19, 2026 and Sep 21, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Difficult to Flush” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Difficult to Flush2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2026Difficult to Flush
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50846503 ↗MalfunctionSep 19, 2026Difficult to Flush
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50833074 ↗
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
- Medline Industries, Inc. DYKMBNDL130Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- MEDLINE PICC0011Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- Centurion IVS3940BCenturion Medical Products Corporation · I.V. start kit2 recalls0 reports
- MEDLINE PICC0013Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- Centurion CVI3805Centurion 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 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