Rebar 105-5082-145Recalls & reported problems

Micro Therapeutics, Inc. · 027 Micro Catheter · Class 2

All models of Rebar (4)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports: 4
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00763000539368), received between Sep 22, 2025 and Nov 20, 2025 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (4 reports).

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

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Physical Resistance/Sticking4

Patient problems

No Clinical Signs, Symptoms or Conditions4

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

MalfunctionNov 20, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
ADDITIONAL INFORMATION WAS RECEIVED. THE CAUSE OF THE RESISTANCE WAS NOT DETERMINED. THERE WAS NO KINK OR DAMAGE OBSERVED ON THE CATHETER, AND THE SOLITAIRE PUSHWIRE WAS NOT KINKED. THE TIP OF THE SOLITAIRE SHEATH WAS SECURED INTO THE HUB OF THE MICROCATHETER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23605777 ↗
MalfunctionNov 13, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE CAUSE OF THE EVENT WAS NOT DETERMINED. A CONTINUOUS SALINE FLUSH WAS ADMINISTERED AND MAINTAINED AS INDICATED IN THE IFU. THERE WAS NO KINK/DAMAGE TO THE CATHETER OBSERVED AFTER REMOVAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23544049 ↗
MalfunctionSep 29, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
ADDITIONAL INFORMATION WAS RECEIVED. THE CAUSE OF THE EVENT WAS NOT DETERMINED. RESISTANCE WAS ENCOUNTERED AT THE DISTAL END OF THE CATHETER. THE COIL CAME OUT OF THE INTRODUCER SHEATH SMOOTHLY. CONTINUOUS SALINE FLUSH WAS ADMINISTERED AND MAINTAINED AS INDICATED IN THE IFU. NO KINK OR DAMAGE TO THE CATHETER WAS OBSERVED AFTER REMOVAL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23168583 ↗
MalfunctionSep 22, 2025Physical Resistance/Sticking; Physical Resistance/Sticking
ADDITIONAL INFORMATION RECEIVED CLARIFIED THAT THE RESISTANCE WAS AT THE DISTAL END OF THE CATHETER. THE CATHETER FLUSH WAS ADMINISTERED PER IFU DURING THE PROCEDURE. THERE WAS NO KINK OR DAMAGE ON THE CATHETER OR SOLITAIRE PUSHWIRE. OF THE SOLITAIRE. THE TIP OF THE SOLITAIRE SHEATH WAS SECURED INTO THE HUB OF THE MICROCATHETER. THE RHV WAS SECURED DURING DELIVERY. THE CAUSE OF THE RESISTANCE WAS NOT DETERMINED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23109973 ↗

Device details

UDI-DI	`00763000539368`
Brand	Rebar
Model	105-5082-145
Company	Micro Therapeutics, Inc.
Product code	KRA · Catheter, continuous flush
Class	Class 2
FDA submission	K210114
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Sep 14, 2023

Device type (GMDN): Vascular microcatheter

A sterile, small-diameter, single-lumen, flexible tube designed for the controlled infusion of fluids (e.g., thrombolytics, diagnostic contrast media) into superselective small vessels (including intracranial, peripheral, or occluded coronary vasculature) for angiography/treatment, and typically also for the delivery of devices (e.g., embolization implants, guidewires) into tortuous vessels or across tight lesions. It may include an ultrasound transducer, a thermal sensor, and a hole for guidewire placement located at the distal tip. It is not a guide-catheter (i.e., is not intended to deliver other catheters or therapeutic leads directly through its lumen). This is a single-use device.

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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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