ARROW IPN037862Recalls & reported problems
Teleflex Incorporated · ARROW ENDURANCE(TM) Extended Dwell Peripheral Catheter System · Class 2
All models of ARROW (1494)
Data updated Oct 16, 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
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10801902132960), received between Feb 8, 2021 and May 6, 2022 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Defective Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- May 19, 2023Open, Classified
Potential for catheter separation or leakage
Z-1826-2023 · Root cause: Under Investigation by firm · Recall details · FDA record ↗
Most reported problems
Device problems
- Defective Component1
- Material Split, Cut or Torn1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2022Material Split, Cut or Torn; Material Split, Cut or Torn
COMPLAINT FOUND IN MAUDE DATABASE REPORTS: "PICC LINE PLACEMENT ATTEMPT RESULTED IN CATHETER THAT WOULD NOT THREAD AND UPON REMOVAL NOTED THE TIP OF CATHETER LOOKED TORN. US AND DOPPLER CONFIRMED CATHETER FRAGMENT IN CEPHALIC VEIN. LINEAR ECHOGENIC STRUCTURE IN THE LEFT CENTRAL UPPER ARM IN THE CEPHALIC VEIN IS CONSISTENT WITH A SMALL PIECE OF RETAINED CATHETER FRAGMENT. VASCULAR CONSULTED."
Patient problems: Foreign Body In Patient
MAUDE report 14312592 ↗MalfunctionFeb 8, 2021Defective Component; Defective Component
THE COMPLAINT IS REPORTED AS: THE USER ATTEMPTED TO ACCESS THE PATIENT'S VEIN WITH THE DEVICE AND WHEN THE USER COULDN'T ACCESS THE VEIN, SHE REMOVED THE ENTIRE N EEDLE/CATHETER FROM THE PATIENT. AFTER REMOVING THE DEVICE, THE USER REMOVED THE CATHETER AND THE SAFETY DID NOT ENGAGE ON THE NEEDLE. NO PATIENT OR USER INJURY OR COMPLICATION REPORTED. THE PATIENT'S CONDITION IS REPORTED AS FINE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11293638 ↗
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- BD Insyte Autoguard 381423Becton, Dickinson And Company · Catheter,intravascular,therapeutic,short-term less than 30 days1 recall528 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 · each recall links to the FDA recall notice
- 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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