Port Access Kit 2632234Recalls & reported problems
Bard Access Systems, Inc. · MiniLoc 22G x .75" PAK · Class 2
All models of Port Access Kit (49)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00801741044410), received between Dec 7, 2022 and Dec 7, 2022 — classified as 1 injury.
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
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Erythema1
- Urticaria1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 7, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED BY PATIENT¿S CARETAKER, THE PATIENT HAD A REACTION TO THE NEEDLE IN THE PORT KIT. PATIENT STATES SHE HAS A NICKEL ALLERGY, ASKING IF WE MAKE A NON-CORNING NEEDLE THAT DOES NOT CONTAIN NICKEL. CALLER STATES SHE WAS USING THE HUBER PLUS NON-CORING NEEDLE IN THE PAST AND DID NOT HAVE ANY ISSUES WITH THIS DEVICE. CALLER DESCRIBING HIVES, RAISED RED AREAS, ITCHING, PUFFINESS NEAR WHERE HER PORT IS LOCATED. RESPONSE: EXPLAINED THAT BOTH THE HUBER PLUS AND MINILOC PORT ACCESS NEEDLES ARE STAINLESS STEEL AND WILL CONTAIN SOME NICKEL. BD DOES NOT MANUFACTURE A NON-CORING NEEDLE THAT DOES NOT CONTAIN NICKEL. DISCUSSED OTHER POSSIBILITIES FOR A REACTION INCLUDING WHICH DRESSING WAS USED AND SKIN PREP LIKE CHLORHEXIDINE. ALSO EXPLAINED HUBER PLUS HAS BEEN DISCONTINUED. OFFERED NON-POWER OPTION, SAFESTEP LH-0029 AND POWER RATED OPTION, 0652234. SUGGESTED SHE DISCUSS THIS FURTHER WITH HER DOCTOR WHO SHOULD BE ABLE TO HELP GET ADDITIONAL SUPPLIES.
Patient problems: Erythema; Urticaria
MAUDE report 15934426 ↗
Other PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR devices
- PowerPort M.R.I., Groshong 9808560Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR3 deaths834 reports
- PowerPort ClearVUE 1608062Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR18 deaths571 reports
- PowerPort ClearVUE 5608062Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR31 deaths542 reports
- PowerPort M.R.I., ChronoFlex 1808000Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR19 deaths513 reports
- PowerPort M.R.I., ChronoFlex 1808060Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR1 recall15 deaths383 reports
- PowerPort M.R.I., Groshong 1808560Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR10 deaths304 reports
- PowerPort M.R.I., ChronoFlex 1829500Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR6 deaths197 reports
- BardPort M.R.I. 0602680Bard Access Systems, Inc. · PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR2 deaths179 reports
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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