Idaho Recalls

2,367 recalls on record affecting Idaho

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.

View recall details →
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.

View recall details →
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.

View recall details →
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.

View recall details →
medical Class II
2017-01-25

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.

View recall details →
medical Class II
2017-02-01

Sekisui Diagnostics P.E.I. Inc. recalls Sekisui Diagnostics Ammonia L3K¿ Assay; Catalog Number: 293-

Certain lots are showing an atypical decrease in optical density (OD) over time, which may result in an impact to performance at the high end of the linear range.

View recall details →
medical Class II
2017-02-01

Acumedia Manufacturers, Inc. recalls Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50K

light precipitate may form in prepared plates of Acumedia Tryptic Soy Agar (7100) Lot# 108166. While there is no change in growth performance of this medium, the formation of particulate matter may be misinterpreted as growth in poured plates thereby leading to inaccurate counts.

View recall details →
medical Class II
2017-02-15

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.

View recall details →
medical Class II
2017-02-15

Invacare Corporation recalls Bariatric Bed - BAR600IVC

The junction box used in the bariatric bed may emit sparks and result in a fire.

View recall details →
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.

View recall details →
medical Class II
2017-02-15

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.

View recall details →
medical Class II
2017-02-15

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.

View recall details →
medical Class III
2017-03-01

Applied Medical Technology Inc recalls AMT Bridle - Nasal Tube Retaining System Used with Nasoga

Expired expiration dates are listed on the pouches.

View recall details →
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%.

View recall details →
medical Class III
2017-03-01

Applied Medical Technology Inc recalls AMT 12 inch Right Angle Feeding Set with Y-Port Used with

Expired expiration dates are listed on the pouches.

View recall details →
medical Class II
2017-03-01

BioMerieux SA recalls ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-4

Potential performance issues. False Susceptible result instead of Intermediate and False Intermediate result with certain methods.

View recall details →
medical Class II
2017-03-01

Custom Medical Specialties, Inc. recalls CMS-2193-R7 and CMS-1911-R3 Custom Biopsy Tray containing a

Sterility of syringe product could not be assured.

View recall details →
medical Class II
2017-03-08

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.

View recall details →
medical Class II
2017-03-08

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.

View recall details →
medical Class II
2017-03-08

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.

View recall details →

Showing 20 of 2,367 recalls. Use search to filter further.