ARROW IPN926648Recalls & reported problems
Teleflex Incorporated · Pressure Injectable Two-Lumen PICC pre-loaded with Arrow(R) NaviCurve(TM) Stylet · Class 2 · Implant
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 10801902212303), received between Mar 9, 2026 and Mar 9, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Leak/Splash” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Leak/Splash1
- Material Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 9, 2026Leak/Splash; Material Split, Cut or Torn
"A 5FR TELEFLEX NAVICURVE PICC HAS FRACTURED ON THE WARD. IT STARTED LEAKING YESTERDAY, I REVIEWED IT AND PROMPTLY REMOVED IT TODAY". ADDITIONAL INFORMATION RECEIVED STATES ". NURSE REQUESTED TO RETRACT PICC DUE TO TIP IRRITATING ENDOCARDIUM CAUSING TACHYCARDIA. RETRACTED 1.5CM TO NEW EXTERNAL LENGTH 9.5CM, BOTH LUMENS FLUSHING AND ASPIRATING, HOWEVER NOTICED SMALL LEAK FROM PINK LUMEN - VAT NURSE DOCUMENTED TO AVOID USING PINK LUMEN. PICC HAD BEEN RARELY USED DURING THIS ADMISSION, PATIENT CANNULATED AND ALL MEDICATIONS GIVEN VIA PIVC. I REVIEWED THE PICC 9/2 - FLUSHED AND ASPIRATED BOTH LUMENS, SMALL LEAK COMING FROM PINK LUMEN. REMOVED AND TESTED TO CONFIRM SPLIT CATHETER - CONFIRMED AROUND 8.5CM EXTERNAL LENGTH". THE DEVICE WAS REMOVED AND REPLACED WITH A NEW CATHETER. THERE WAS NO PATIENT HARM OR INJURY. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "SATISFACTORY".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24546057 ↗
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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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