Vermont Recalls

1,390 recalls on record affecting Vermont

medical Class II
2017-01-18

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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medical Class II
2017-01-18

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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medical Class II
2017-01-18

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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medical Class II
2017-01-25

Meridian Bioscience Inc recalls PREMIER EHEC and PREMIER EHEC Bulk.

Internal testing has demonstrated that the indicated kit lots produce false positive results when tested with some broth specimens.

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medical Class II
2017-02-15

AtriCure, Inc. recalls AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgr

A complaint of the PRO2 jaw breaking prior to surgery being performed.

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medical Class II
2017-02-22

Philips Medical Systems (Cleveland) Inc recalls BrightView XCT

The intended use listed in the English and localized language IFUs for BrightView XCT systems did not match the intended use documented in the 510K submission.

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medical Class II
2017-02-22

Philips Medical Systems (Cleveland) Inc recalls BrightView X upgraded to XCT 882454

The intended use listed in the English and localized language IFUs for BrightView XCT systems did not match the intended use documented in the 510K submission.

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medical Class II
2017-03-01

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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medical Class II
2017-03-08

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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medical Class II
2017-03-29

Merge Healthcare, Inc. recalls Merge Cardio software using EchoIMS. The firm name on the l

A situation can occur allowing two physicians to access the same study report in EchoIMS when launched from the Cardio Study List without receiving the read-only notification prompt.

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medical Class II
2017-03-29

Merge Healthcare, Inc. recalls Merge Cardio software with Issuer of Patient ID (IPID). The

For sites using the Issuer of Patient ID (IPID), the system will display the study list and images from different patients with different IPIDs as though they are for the same patient if they all have the first name, last name, and medical record number in common.

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medical Class II
2017-04-19

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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medical Class III
2017-04-26

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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medical Class II
2017-05-10

Richard-Allan Scientific Company recalls Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Sha

Methylene Blue, Solution #3 in the Kwik Diff Kit was not Methylene Blue but Crystal Violet instead.

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medical Class II
2017-05-17

Arthrex, Inc. recalls Anthrex SpeedBridge Implant System with PEEK SwiveLock Self

Some eyelets broke from SwiveLock Anchor on insertion.

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medical Class II
2017-05-17

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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medical Class II
2017-05-17

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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medical Class II
2017-05-17

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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medical Class II
2017-05-17

Arthrex, Inc. recalls Anthrex SpeedBridge Implant System with BioComposite SwiveLo

Some eyelets broke from SwiveLock Anchor on insertion.

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medical Class II
2017-05-17

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 1,390 recalls. Use search to filter further.