Lifeport LPS5057Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI H787LPS50570), received between Jan 17, 2025 and Jan 17, 2025 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K953529); they may or may not involve this specific model.

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJan 17, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  ON OR ABOUT (B)(6) 2014, PLAINTIFF UNDERWENT PLACEMENT OF THE ANGIODYNAMICS LIFEPORT VASCULAR ACCESS PORT, REFERENCE NUMBER (B)(4), LOT NUMBER 606481. THE DEVICE WAS IMPLANTED BY DR. (B)(6), M.D., AT (B)(6) HOSPITAL IN (B)(6) FOR THE PURPOSE OF ONGOING CHEMOTHERAPY FOR HIS CANCER. ON OR ABOUT (B)(6) 2015, PLAINTIFF PRESENTED HIMSELF (B)(6) CENTER WHERE IT WAS DETERMINED HE WAS SUFFERING FROM INFECTION AT THE PORT SITE AND HIS PORT WAS SUBSEQUENTLY REMOVED.

  Patient problems: Unspecified Infection

  MAUDE report 21177650 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K953529. One submission often covers many models, so check the product and lot details in each record.

• Z-0256-05 · Sep 20, 2004 · Terminated
  LifePort, Dual Lumen Profile Plastic Dual Port with Poly Urethane Catheter Kit, Product Code/REF: LPS 7255, Manufactured by: Horizon Medical Products, Inc., One Horizon Way, P.O. B