Bayer Medical Care Inc.
1 Bayer Drive, INDIANOLA, PA, US
Registered product codes
15 product codes
Recent MDR events
752 on file
- MEDRAD® STELLANT FLEX CT INJECTION SYSTEM WITH CERTEGRA® WORKSTATIONJul 21, 2026Injury2520313-2026-00020
- MEDRAD® STELLANT CT INJECTION SYSTEMJun 22, 2026Death2520313-2026-00019
- MEDRAD® MARK 7 ARTERION INJECTION SYSTEMJun 9, 2026Malfunction25443532
- MEDRAD® STELLANT FLEX CT INJECTION SYSTEM WITH CENTEGRA WORKSTATIONMay 28, 2026Injury2520313-2026-00016
- MEDRAD® STELLANT CT INJECTION SYSTEM WITH CENTEGRA WORKSTATIONMay 7, 2026Injury2520313-2026-00015
- MEDRAD® STELLANT DUAL CT INJECTORMay 1, 2026Injury2520313-2026-00014
- MEDRAD® STELLANT DUAL CT INJECTORApr 15, 2026Injury2520313-2026-00012
- STELLANT DUAL CT INJECTORApr 2, 2026Injury2520313-2026-00011
- MEDRAD® STELLANT FLEX SYRINGE KITMar 19, 2026Malfunction24637969
- STELLANT DUAL CT INJECTORMar 12, 2026Injury2520313-2026-00009
Recalls
9 on file
- Open, ClassifiedJun 3, 2026
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.
View FDA record ↗ - Open, ClassifiedJan 6, 2023
Black specks may be present on the packaged needles
View FDA record ↗ - TerminatedUnknown
Bayer has received reports of loose particulate in the filter when the dust cap is removed. Bayer conducted further testing confirming the dust cap may generate particulate which may potentially enter the fluid path.
View FDA record ↗ - TerminatedUnknown
Labeling error: MEDRAD Mark 7 Arterion Injection System Syringes (ART 700 SYR) labeled as Twist & Go Syringes (TAG 150 SYR)
View FDA record ↗ - TerminatedUnknown
Specific lots of MEDRAD Stellant FLEX 150 mL syringe kits may have holes and/or cracks that have the potential to allow fluid to leak out of the syringe.
View FDA record ↗ - TerminatedUnknown
If the head mount knob is not properly tightened and the operator directly uses the injector head to move the unit, it may become disengaged, causing the injector head to become loose or fall.
View FDA record ↗ - TerminatedUnknown
The torque wrench used on the ceiling column assembly during a recent service visit was outside of the torque specification, potentially overtightening the bolts. The overtightening of bolts may compromise the structural integrity of the system which could lead to the OCS disengaging from the ceiling mount and this may cause injury to the patient or the operator.
View FDA record ↗ - TerminatedUnknown
The torque wrench used on the ceiling column assembly during a recent service visit was outside of the torque specification, potentially overtightening the bolts. The overtightening of bolts may compromise the structural integrity of the system which could lead to the OCS disengaging from the ceiling mount and this may cause injury to the patient or the operator.
View FDA record ↗ - TerminatedUnknown
The torque wrench used on the ceiling column assembly during a recent service visit was outside of the torque specification, potentially overtightening the bolts. The overtightening of bolts may compromise the structural integrity of the system which could lead to the OCS disengaging from the ceiling mount and this may cause injury to the patient or the operator.
View FDA record ↗
Compliance history
Matched by FEI 2520313.
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.