ARROW IPN920059Recalls & reported problems
Teleflex Incorporated · Pressure Injectable One-Lumen PICC with 80 cm Wire · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801902192636), received between Mar 30, 2026 and Mar 30, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Patient-Device Incompatibility” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Patient-Device Incompatibility1
Patient problems
- Pain1
- Swelling/ Edema1
- Thrombosis/Thrombus1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 30, 2026Patient-Device Incompatibility
IT WAS REPORTED "PICC INSERTED ON (B)(6) 2026 IN RIGHT BASILIC VEIN. IT WAS CONFIRMED ON THE (B)(6) 2026 THAT THE PATIENT HAD DEVELOPED A THROMBUS IN THEIR UPPER ARM. PICC IS STILL IN THE PATIENT". THE PATIENT EXPERIENCED PAIN AND SWELLING IN THE RIGHT ARM. THE PATIENT REQUIRED ANTICOAGULANT THERAPY. THERE WAS NO PATIENT HARM OR INJURY. NO MEDICAL INTERVENTION REQUIRED. THE PATIENT'S CURRENT CONDITION IS REPORTED AS "FINE".
Patient problems: Pain; Swelling/ Edema; Thrombosis/Thrombus
MAUDE report 24729037 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.