ARROW IPN920647Recalls & reported problems
Teleflex Incorporated · ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10801902196368), received between Mar 25, 2023 and May 2, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Separation” (2 reports).
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
- Material Separation2
Patient problems
- Foreign Body In Patient2
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 2, 2023Material Separation; Material Separation
NURSE NOTICED THE LINE WAS NOT FLUSHING CORRECTLY 2 DAYS AFTER INSERTION. THE NURSE DID NOT REMOVE THE LINE. THE NURSE LEFT THE LINE IN FOR ANOTHER 2-3 DAYS. THE NURSE PULLED THE LINE TO DISCONTINUE. UPON REMOVAL, THE HUB OF THE CATHETER CAME OUT, WITH THE CATHETER LEFT DWELLING AND REMAINING IN THE PATIENT. THE PATIENT HAD TO GO TO THE OPERATING ROOM TO REMOVE FOREIGN BODY.
Patient problems: Foreign Body In Patient
MAUDE report 16857581 ↗InjuryMar 25, 2023Material Separation; Material Separation
IT WAS REPORTED AFTER UNSUCCESSFUL ATTEMPT IN THE LEFT ANTERIOR FOREARM FOR AN ULTRASOUND PLACED IV, UPON REMOVAL PART OF THE CATHETER REMAINED UNDER THE SKIN. THE PIECE OF CATHETER WAS REMOVED (METHOD UNKNOWN) AND ANOTHER CATHETER WAS PLACED SUCCESSFULLY. IT WAS REPORTED THE PATIENT EXPERIENCED PAIN.
Patient problems: Foreign Body In Patient; Pain
MAUDE report 16616714 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.