AllPoints Port Access System PowerLoc AN652034GRecalls & reported problems
Bard Access Systems, Inc. · AllPoints Port Access System PowerLoc 20G x 0.75 inch + GuardIVa · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00801741215452), received between May 14, 2025 and Aug 18, 2025 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (6 reports).
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.
Reports received per month
Most reported problems
Device problems
- Loss of or Failure to Bond6
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Erythema1
- Infiltration into Tissue1
- Swelling/ Edema1
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED THAT A PATIENT CAME IN TODAY WITH DRESSING LIFT. PATIENT HAD SAME EXPERIENCE WITH PREVIOUS DRESSING IN JUNE. NO ADVERSE EVENTS HAVE BEEN REPORTED AT THIS TIME. THIS REPORT ADDRESSES THE EVENT IN JUNE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22835411 ↗MalfunctionAug 18, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED THAT A PATIENT CAME IN TODAY WITH DRESSING LIFT. PATIENT HAD SAME EXPERIENCE WITH PREVIOUS DRESSING IN (B)(6). NO ADVERSE EVENTS HAVE BEEN REPORTED AT THIS TIME. THIS REPORT ADDRESSES THE CURRENT EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22835406 ↗MalfunctionJun 3, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED BY CUSTOMER THAT THE PATIENT'S SENTRINEX DRESSING HAD LIFTED. THE PATIENT EXPERIENCED INFILTRATION. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: Erythema; Infiltration into Tissue; Swelling/ Edema
MAUDE report 22136243 ↗MalfunctionMay 27, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED BY CUSTOMER THAT HAD SEVERAL INSTANCES OF THE SENTRINEX DRESSING INCLUDED IN ALLPOINTS LIFTING. PATIENT'S DRESSING HAD LIFTED AND POSED AN INFECTION RISK. IT WAS REPORTED THIS OCCURRED WITH THREE PATIENTS. THIS REPORT ADDRESSES ALL THREE PATIENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22090745 ↗MalfunctionMay 21, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED THAT THEY HAD PLACED A SENTRINEX DRESSING ON A HOME-INFUSION CADD-PUMP PATIENT. THE DRESSING WAS LIFTING WHEN THE PATIENT RETURNED TO THE INFUSION CENTER. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22064880 ↗MalfunctionMay 14, 2025Loss of or Failure to Bond; Loss of or Failure to Bond
IT WAS REPORTED BY THE CUSTOMER THAT THE PATIENT WAS GIVEN A SENTRINEX DRESSING DURING A PORT ACCESS PROCEDURE. DURING THE PROCESS OF GOING HOME AND RETURNING TO THE INFUSION CENTER, THE DRESSING LIFTED. WHEN THE PATIENT RETURNED, THE DRESSING WAS NOT OCCLUSIVE. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22020425 ↗
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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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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