Centurion IVS1890Recalls & reported problems
Centurion Medical Products Corporation · IV START INSERTION KIT · Class 2
- 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 10653160355557), received between Sep 29, 2026 and Sep 29, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
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 29, 2026Break
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50934237 ↗
Other I.V. start kit devices
- Medline Industries, Inc. DYKM1000BMedline Industries, Inc. · I.V. start kit3 recalls0 reports
- Medline Industries, Inc. CDS860014PMedline Industries, Inc. · I.V. start kit3 recalls0 reports
- MEDLINE DYNJ68937AMedline Industries, Inc. · I.V. start kit2 recalls2 reports
- MEDLINE DYNDV2536Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- Centurion CVI4340Centurion Medical Products Corporation · I.V. start kit2 recalls0 reports
- MEDLINE STCVC2015AMedline Industries, Inc. · I.V. start kit2 recalls0 reports
- Medline Industries, Inc. DYNDV2518Medline Industries, Inc. · I.V. start kit2 recalls0 reports
- MEDLINE PICC0012Medline Industries, Inc. · I.V. start kit2 recalls0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.