AllPoints Port Access System PowerLoc Max AN142075GRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00801741119316), received between Oct 31, 2024 and Feb 6, 2026 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Material Deformation” (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.

• InjuryFeb 6, 2026Adverse Event Without Identified Device or Use Problem

  ADDITIONAL INFORMATION RECEIVED 28 JAN. 2026. THE KITS WERE SUPPOSED TO HAVE THE BALLOONED DRESSING THAT DOES NOT STICK TO THE HUB OF THE NEEDLE. INSTEAD, THE DRESSING WAS SUBSTITUTED WITH A REGULAR TEGADERM WITH CHG, WHICH STUCK TO THE ENTIRE HUBER NEEDLE AND WOULD NOT ALLOW THE SAFETY TO ENGAGE. THE NURSE WAS PEELING THE DRESSING OFF WHEN THE NEEDLE CAME OUT OF THE PATIENT AND SHE WAS STUCK. THE PATIENT DID NOT HAVE ANY BLOOD BORNE DISEASES, BUT BLOOD WORK WAS COMPLETED FOR THE NURSE AS A PRECAUTION. THERE WAS NO LONG TERM HARM REPORTED.

  Patient problems: Needle Stick/Puncture

  MAUDE report 24277323 ↗
• MalfunctionOct 31, 2024Material Deformation; Material Deformation

  IT WAS REPORTED BY THE CUSTOMER, POWERLOC MAX NEEDLE FROM WITHIN ALL POINTS KIT BENT WHEN ACCESSED PATIENT. CUSTOMER SAYS THE NEEDLE WAS NOT INITIALLY BENT AND IS UNSURE AT WHAT POINT THE NEEDLE BENT. 10/10/2024 - THE SAFETY MECHANISM FAILED TO ACTIVATE ON THE RETURNED DEVICE DURING EVALUATION.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20580842 ↗