Alaska Recalls
1,131 recalls on record affecting Alaska
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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Stryker Sustainability Solutions recalls Reprocessed Electrophysiology Catheter Cables Catalog Numbe
A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.
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Stryker Sustainability Solutions recalls Reprocessed Ablation Catheter Cable Catalog Number: CR3425C
A breach in the sterile packaging may have occurred resulting in potentially non-sterile product.
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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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Philips Electronics North America Corporation recalls Philips Cisco 3850 layer 3 switch, 865339 model WS-C3850-12S
May experience a loss of centralized monitoring.
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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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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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Tosoh Bioscience, Inc. recalls Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
The device defect associated with this recall may result in HbA1c values with a negative bias in patients with the hemoglobin variants C, D, E and S. The negative bias occurs at the higher levels of HbA1c, e.g. 9%, but not at the diagnostic medical decision point of 6.5%.
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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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Smiths Medical ASD Inc. recalls CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Smiths Medical has become aware that the drawing on the Instructions for Use (IFU) on certain yellow striped CADD¿ Administration Sets (part number 21-7339-24), incorrectly represent the actual filter size of the product. Although the text description on the IFU correctly identifies the product to include a 0.2 micron filter, the illustration on the IFU identifies the filter size as 2.0 microns.
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Teleflex Medical recalls Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Some of the individual unit packaging (pouches) may be missing the lot number an expiration date.
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Arthrex, Inc. recalls Anthrex SpeedBridge Implant System with PEEK SwiveLock Self
Some eyelets broke from SwiveLock Anchor on insertion.
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Arthrex, Inc. recalls Anthrex Bio Composite SwiveLock SP Vented, 4.75 mm x 24.5 mm
Some eyelets broke from SwiveLock Anchor on insertion.
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Arthrex, Inc. recalls Anthrex PEEK SwiveLock SP Vented, 4.75 mm x 24.5 mm, Self-Pu
Some eyelets broke from SwiveLock Anchor on insertion.
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Arthrex, Inc. recalls Anthrex PEEK SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punc
Some eyelets broke from SwiveLock Anchor on insertion.
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Arthrex, Inc. recalls Anthrex SpeedBridge Implant System with BioComposite SwiveLo
Some eyelets broke from SwiveLock Anchor on insertion.
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Arthrex, Inc. recalls Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punch
Some eyelets broke from SwiveLock Anchor on insertion.
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Showing 20 of 1,131 recalls. Use search to filter further.