ARROW IPN037860Recalls & reported problems
Teleflex Incorporated · ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902132922), received between Dec 21, 2018 and Dec 21, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Component Missing” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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. How this data works · Data updated Oct 13, 2026.
Recalls naming this device
- May 19, 2023Open, Classified
Potential for catheter separation or leakage
Z-1826-2023 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Component Missing1
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.
InjuryDec 21, 2018Component Missing
PERIPHERAL IV PLACED VIA ULTRASOUND USING A TECHNIQUE CALLED ACCELERATED SELDINGER(AST). THE NURSE RETRACTED THE DEVICE BY GRASPING THE CATHETER PULLING IT BACK OVER THE NEEDLE APPROXIMATELY 0.5 CM. ON INSPECTION OF THE DEVICE 0.5 CM WAS MISSING FROM THE END OF THE CATHETER. UNABLE TO VISUALLY DETERMINE IF IT FELL ON THE BED ON REMOVAL, THE RN RESPONDED IMMEDIATELY NOTIFYING THE NURSE MANAGER FOR DIRECTION. THEY PHYSICIAN WAS NOTIFIED AND X-RAYS WERE ORDERED AS RECOMMENDED. THE MEDICAL DIRECTOR WAS NOTIFIED AND COLLABORATED WITH THE CARE AND TREATMENT RECOMMENDATIONS. THE FOREIGN BODY WAS IDENTIFIED IN THE SOFT TISSUE VS THE VESSEL, VIA X-RAY OF ARM. CHEST X-RAY WAS NEGATIVE FOR FOREIGN BODY. A CT SCAN WAS DONE TO FURTHER DEFINE THE LOCATION OF THE CATHETER TIP. THE PATIENT WAS MADE NPO FOR LOCAL ANESTHETIC REMOVAL IN OPERATING ROOM . PATIENT TOLERATED THE REMOVAL PROCEDURE AND WAS DISCHARGED TO HOME IN STABLE CONDITION THE FOLLOWING DAY.
Patient problems: No Code Available
MAUDE report 8194434 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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