Bard Access Systems, Inc.
605 North 5600 West, Salt Lake City, UT, US
Registered product codes
45 product codes
Recent MDR events
2,409 on file
- DuoGlide catheterJul 28, 2026Malfunction50052422
- PowerPICC ProvenaJul 28, 2026Malfunction50052453
- PowerPICC ProvenaJul 28, 2026Malfunction50052455
- HUBER PWERLOCMAX 20G 3/4" 0142075Jul 16, 2026InjuryMW5190822
- MIDLINE GUIDEWIREJul 14, 2026MalfunctionMW5190730
- POWERGLIDE MIDLINE CATHETERJul 9, 2026Death25761705
- STATLOCKJun 30, 2026MalfunctionMW5190067
- BD POWERPICC CATHETERJun 29, 2026MalfunctionMW5189955
- POWERPICC HF CATHETERJun 25, 2026Malfunction25620005
- POWERPICCJun 23, 2026Malfunction25592692
Recalls
85 on file
- Open, ClassifiedAug 14, 2026
After placement of intraosseous (IO) needle sets, used when intravenous access is difficult or impossible to obtain in emergent, urgent, or medically necessary cases, users may experience difficulty/inability to remove obturator, due to it locking to the needle hub, due to out-of-tolerance dimensions and IFU unclarity, which may result in new needle placement, which may result in delayed therapy
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗ - Open, ClassifiedJul 2, 2026
Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.
View FDA record ↗
Compliance history
Matched by FEI 3006260740.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.