Carefusion 2200, Inc.
75 North Fairway Drive, Vernon Hills, IL, US
Registered product codes
64 product codes
Recent MDR events
358 on file
- BD CLIPVAC DISPOSABLE FILTER ASSEMBLY- BD SURGICAL CLIPPERJul 21, 2026Malfunction25889613
- BD INSYTE AUTOGUARDJul 21, 2026InjuryMW5190943
- BD 20 ML STERILE LUER-LOCK SYRINGEJul 21, 2026MalfunctionMW5190946
- JAMSHIDIJul 9, 2026Malfunction25763063
- BD ALARIS PRIMARY PUMP SETJun 29, 2026MalfunctionMW5189969
- ALARIS PUMP INFUSION SETJun 22, 2026MalfunctionMW5189727
- SAFE-T-CENTESIS DRAINAGE SYSTEMJun 8, 2026Malfunction25427559
- SAFE-T-CENTESISMay 14, 2026Malfunction25169052
- THORA/PARA KITMay 11, 2026Malfunction25136160
- BD ALARIS PUMP MODULE INFUSION SETMay 4, 2026OtherMW5187570
Recalls
114 on file
- Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗ - Open, ClassifiedSep 30, 2024
Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.
View FDA record ↗
Compliance history
Matched by FEI 3008002452.
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.