Recon SCCTO110ATRecalls & reported problems
Bard Peripheral Vascular, Inc. · Recon Support Catheter, Angled, Tapered, 110cm · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741201295), received between Jul 26, 2022 and Nov 19, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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
- Device-Device Incompatibility1
- Improper or Incorrect Procedure or Method1
- Material Deformation1
- Material Frayed1
- Retraction Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 19, 2024Retraction Problem; Device-Device Incompatibility; Material Deformation; Retraction Problem; Device-Device Incompatibility; Material Deformation
IT WAS REPORTED THAT DURING A RECANALIZATION PROCEDURE VIA CONTRALATERAL APPROACH, THE RECON ALLEGEDLY WAS NOT GETTING INTO THE CROSSER. IT WAS FURTHER REPORTED THAT THE CROSSER ALLEGEDLY DISCONNECTED FROM THE RECON. REPORTEDLY, THEY HAD TO PULL EVERYTHING OUT. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20721469 ↗MalfunctionJul 26, 2022Material Frayed; Improper or Incorrect Procedure or Method; Material Frayed; Improper or Incorrect Procedure or Method
IT WAS REPORTED THAT DURING A RECANALIZATION PROCEDURE, THE TIP OF THE DEVICE ALLEGEDLY GOT FRAYED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15101488 ↗
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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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