Teleport Microcatheter 220-15-1000URecalls & reported problems
OrbusNeich Medical (ShenZhen) Co., Ltd. · Caatheter, Percutaneous · Class 2
Data updated Oct 18, 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 06934955943065), received between Mar 24, 2019 and Mar 24, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Advance” (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 18, 2026.
Most reported problems
Device problems
- Failure to Advance1
- Fracture1
- Stretched1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 24, 2019Fracture; Stretched; Failure to Advance
THE MICROCATHETER COULD NOT CROSS THE LESION AND BECAME STUCK AT THE SAME LOCATION AS THE PREVIOUS DEVICE. ADDITIONAL FORCE WAS APPLIED TO REMOVE THE MICROCATHETER AND THE MICROCATHETER FRACTURED AND STRETCHED DURING REMOVAL. THE PROCEDURE WAS COMPLETED WITH ANGIOPLASTY AND ATHERECTOMY. THE VESSEL WAS 95% STENOTIC WITH A DIAMETER OF 3.5MM AND SEVERE CALCIFICATION.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8446663 ↗
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- WATCHMAN™ TruSeal™ Access System M635TU70020Boston Scientific Corporation · Catheter, percutaneous1 recall11 deaths217 reports
- Lantern Delivery Catheter PXSLIMLAN135T45Penumbra, Inc. · CATHETER, PERCUTANEOUS220 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 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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