ARROW IPN033577Recalls & reported problems
Teleflex Incorporated · RIC(R) Rapid Infusion Catheter Exchange Set · Class 2
All models of ARROW (1494)
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 00801902001368), received between Oct 18, 2019 and Oct 18, 2019 — classified as 1 malfunction.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 18, 2019Adverse Event Without Identified Device or Use Problem
A PROCEDURE BY ANESTHESIOLOGIST WAS PERFORMED: INSERTION OF A RAPID INFUSION CATHETER INTO THE LEFT UPPER EXTREMITY USING A GUIDEWIRE. THE PATENCY OF THE IV WAS CHECKED BY ULTRASOUND AND FLUSHED WITH SALINE. THE FOLLOWING DAY, AN X-RAY THE FOLLOWING CONFIRMED THE GUIDEWIRE WAS RETAINED AND WAS SEEN IN THE LEFT ARM RUNNING ALONG THE LEFT SIDED THORACIC SPINE. THE PATIENT WAS TAKEN TO INTERVENTIONAL RADIOLOGY FOR REMOVAL.
Patient problems: No Code Available
MAUDE report 9207711 ↗
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- Swartz™ 407451St. Jude Medical, Inc. · INTRODUCER, CATHETER5 deaths728 reports
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- Agilis™ G408318St. Jude Medical, Inc. · INTRODUCER, CATHETER333 reports
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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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