MEDLINE STCVC01145BRecalls & reported problems
Medline Industries, Inc. · VANTEX 7FR 3L 16CM CVC BUNDLE · Class 2
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-2195-2023 · 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-2304-2023 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗
Other Catheter introducer kit devices
- Centurion CVI4510Centurion Medical Products Corporation · Catheter introducer kit2 recalls0 reports
- Medline Industries, Inc. STCVC2000Centurion Medical Products Corporation · Catheter introducer kit2 recalls0 reports
- Centurion ART905Centurion Medical Products Corporation · Catheter introducer kit1 recall0 reports
- Medline Industries, Inc. STCVC2020Centurion Medical Products Corporation · Catheter introducer kit1 recall0 reports
- Medline Industries, Inc. I505BF9CCenturion Medical Products Corporation · Catheter introducer kit1 recall0 reports
- Medline Industries, Inc. I550BF6CCenturion Medical Products Corporation · Catheter introducer kit1 recall0 reports
- Centurion I300F85Centurion Medical Products Corporation · Catheter introducer kit12 reports
- Centurion I505BF9Centurion Medical Products Corporation · Catheter introducer kit2 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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