Port Access NeedleRecalls & reported problems across all models
Bard Access Systems, Inc. · 122 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Port Access Needle models — page 2
122 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Port Access Needle SHW20-100YSSet, administration, intravascular2 reports
- Port Access Needle 573112Set, administration, intravascular1 report
- Port Access Needle 0632050Set, administration, intravascular1 report
- Port Access Needle 0642010Set, administration, intravascular1 report
- Port Access Needle 0642034Set, administration, intravascular1 report
- Port Access Needle 0651910Set, administration, intravascular1 report
- Port Access Needle 0661910Set, administration, intravascular1 report
- Port Access Needle 0662034Set, administration, intravascular1 report
- Port Access Needle 0672015Set, administration, intravascular1 report
- Port Access Needle S02319-10Set, administration, intravascular1 report
- Port Access Needle 012012Set, administration, intravascular1 report
- Port Access Needle 0603300Needle, hypodermic, single lumen1 report
- Port Access Needle S02120-10Set, administration, intravascular1 report
- Port Access Needle S02120-75Set, administration, intravascular1 report
- Port Access Needle SH22-75YSSet, administration, intravascular1 report
- Port Access Needle SHG19-75YSet, administration, intravascular1 report
- Port Access Needle SHG20-75YSet, administration, intravascular1 report
- Port Access Needle SHG22-100Set, administration, intravascular1 report
- Port Access Needle SHW19-75YSet, administration, intravascular1 report
- Port Access Needle SHW19-75YSSet, administration, intravascular1 report
- Port Access Needle SHW20-100Set, administration, intravascular1 report
- Port Access Needle SHW20-100YSet, administration, intravascular1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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