Centurion CVI4180 (UDI 10653160284451)Recalls & reported problems
Centurion Medical Products Corporation · VASCULAR ACCESS INSERTION KIT · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 2
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
2 FDA recall records name this device's identifier, 2 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 16, 2026.
Recalls naming this device
- May 18, 2023Open, Classified
Probe covers for use during diagnostic ultrasound procedures may have an inadequate barrier at the seams.
Z-2199-2023 · Root cause: Device Design · Recall details · FDA record ↗
- May 15, 2023Open, Classified
Potential for the labeled sterile ultrasound gel component within packs to not meet sterility specifications.
Z-2322-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other TRAY, SURGICAL devices
- MEDLINE DYNDA2526Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1534Medline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYNDH1470BMedline Industries, Inc. · TRAY, SURGICAL3 recalls0 reports
- Centurion MNS11625Centurion Medical Products Corporation · TRAY, SURGICAL3 recalls0 reports
- MEDLINE DYKM1756AMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE SPEC0291BMedline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYNDC3188Medline Industries, Inc. · TRAY, SURGICAL2 recalls0 reports
- MEDLINE DYNDH1542Medline Industries, Inc. · TRAY, SURGICAL2 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
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- 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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