AllPoints Port Access System PowerLoc Max AN142075BRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741215209), received between Apr 2, 2025 and Mar 24, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Activation Problem” (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 18, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 24, 2026Tear, Rip or Hole in Device Packaging

  IT WAS REPORTED THAT CUSTOMER RECEIVED SEVERAL DAMAGED ITEMS. A SPECIFIC NUMBER OF AFFECTED DEVICES OR PATIENTS WAS NOT PROVIDED BY THE COMPLAINANT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24681778 ↗
• InjuryApr 2, 2025Activation Problem; Activation Problem

  IT WAS REPORTED BY THE CUSTOMER ¿AT APPROXIMATELY 12:10 I REMOVED A PATIENT'S PORT NEEDLE ACCESS FROM THEIR CHEST AND PLACE THE LOCKED, PRESUMED RETRACTED NEEDLE ON THE BEDSIDE TABLE. PATIENT WAS DISCHARGED AND I RETURNED TO CLEAN UP HER CHAIR. UPON DISCARDING PORT NEEDLE MY RIGHT THUMB WAS PUNCTURED BY THE NEEDLE. UPON FURTHER INSPECTION IT APPEARS THAT THE SAFETY FAILED ON THE DEVICE. IN THE FULLY LOCKED POSITION THE NEEDLE WAS PARTIALLY EXPOSED ON THE PLATE. CLINIC WAS NOTIFIED AND LABS WERE ADDED ON TO PATIENT'S PREVIOUSLY DRAWN BLOOD FROM EARLIER IN THE DAY."

  Patient problems: Needle Stick/Puncture

  MAUDE report 21752936 ↗