Centurion IVS1945Recalls & reported problems
Centurion Medical Products Corporation · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10653160269441), received between Sep 9, 2026 and Sep 9, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fluid/Blood Leak” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak1
- Loose or Intermittent Connection1
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.
MalfunctionSep 9, 2026Fluid/Blood Leak; Loose or Intermittent Connection
It was reported that "our Iv Securement Kits leaking fluids" and "when he screws on the insyte needle to the pigtail it comes loose even after its tight".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50693684 ↗
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.
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