Recon SCCTO110TRecalls & reported problems
Bard Peripheral Vascular, Inc. · Recon Support Catheter, Straight, Tapered, 110cm · 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 00801741201301), received between Aug 9, 2023 and Aug 9, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (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.
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Entrapment of Device1
- Material Deformation1
- Material Frayed1
- Retraction 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.
MalfunctionAug 9, 2023Entrapment of Device; Material Frayed; Retraction Problem; Detachment of Device or Device Component; Material Deformation; Entrapment of Device; Material Frayed; Retraction Problem; Detachment of Device or Device Component; Material Deformation
IT WAS REPORTED THAT DURING A RECANALIZATION PROCEDURE IN THE TIBIOPERONEAL TRUNK, THE SUPPORT CATHETER WAS ALLEGEDLY FOUND TO BE LODGED AND WOULD NOT ADVANCE TO REMOVE FROM THE PATIENT¿S PERONEAL ARTERY WITH THE CATHETER. REPORTEDLY, THE DEVICE WAS REMOVED FROM THE BODY WITH EXTREME DIFFICULTY. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17485878 ↗
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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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