Medline Industries, Inc. DYNDV2464ARecalls & reported problems
Medline Industries, Inc. · OUTPATIENT 2 TO 5 YEARS · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10195327065911), received between Nov 24, 2025 and Nov 24, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Integrity Problem” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Nov 26, 2025Class IIOpen, Classified
Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.
Z-1056-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Most reported problems
Device problems
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 24, 2025Material Integrity Problem; Material Integrity Problem
"Y-PIECE BROKEN OFF".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23632097 ↗
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 · each recall links to the FDA recall notice
- 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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