Hawaii Recalls
2,001 recalls on record affecting Hawaii
GE OEC Medical Systems, Inc recalls The OEC 9900 Elite mobile fluoroscopy system is designed to
GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.
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GE OEC Medical Systems, Inc recalls OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 680
GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.
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GE OEC Medical Systems, Inc recalls OEC 9800. MDL Numbers: D222250, D141598 The OEC 9800 is des
GE Healthcare Surgery announces a voluntary field action for the OEC MiniView 6800, OEC 9900 Elite, and OEC 9800 because the workstation power cable assembly can result in intermittent power cord failures.
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DICOM GRID INC recalls Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R S
A software error caused the window/level to become the same in one series regardless if the image had different levels; image results have a washed-out grey appearance.
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The Binding Site Group, Ltd. recalls Human Lambda Free SPAPlus Kit Product Code: LK018.S Fr
Calibration curve activity has increased over time in the kit lots listed.
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INO Therapeutics (dba Ikaria) recalls Mallinckrodt Pharmaceuticals INOmax DSIR Plus delivery syste
Mallinckrodt discovered that some devices may have been manufactured with an out-of-tolerance manometer which can result in in an inaccurate proportional valve calibration table in an affected device.
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Invacare Corporation recalls Foot Section - BAR5490IVC
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Merge Healthcare, Inc. recalls Merge PACS software. The firm name on the label is Merge He
Potential exists for an incorrect patient image being displayed which could result in the delay in diagnosis or treatment.
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Teleflex Medical recalls Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and She
Labeling inconsistency - units labeled with a 7mm tube may contain a size 6.5mm tube, and units labeled 7.5mm tube may contain a size 5.5mm tube.
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Invacare Corporation recalls Bariatric Bed - BAR600IVC
The junction box used in the bariatric bed may emit sparks and result in a fire.
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Invacare Corporation recalls Junction Box - 1104343 and 1193560
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Invacare Corporation recalls Bariatric Bed - BARPKG-IVC 1633
A quality issue with the junction box used in the bariatric bed junction that may omit sparks and result into a fire.
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Mckesson Medical Imaging recalls McKesson Radiology 12.2 - Picture Archive Communication Syst
Issue for customers that use an EMR login or legacy web URL login or legacy web URL login for McKesson Radiology PACS that may result in missing images in a newly imported study, and/or study imports that remain in an "in-progress" status.
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Cook Inc. recalls Flexor Radial Access Set, Individual product is packaged in
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls Check-Flo Introducer Hausdorf-Lock Atrial, Individual produc
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls Check-Flo Performer Introducer Set, Individual product is pa
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls Check-Flo Performer Introducer, Individual product is packag
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls Check-Flo Hemostasis Assembly, Individual product is package
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls TriForce Peripheral Crossing Set, Individual product is pack
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Cook Inc. recalls Micropuncture Check-Flo Performer Introducer Set, Individual
Devices using a specific hemostatic valve design, referred to as a blue valve or polyisoprene valve, have an increase in reports of blood loss associated with the devices which could result in delay in procedure and blood loss from patients.
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Showing 20 of 2,001 recalls. Use search to filter further.