Product Recalls in Idaho

Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,436 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,436 in last 12 months

Showing 1880118820 of 27,833 recalls

Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition Flash system Recalled by Siemens Medical Solutions USA,...

The Issue: Hardware issue that may expose the user to a potential risk for serious...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Definition AS Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: A problem can occur with the small light marker windows, used for the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Beckman Coulter Inc.

Recalled Item: AQUIOS Lyse Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...

The Issue: Beckman Coulter is recalling the AQUIOS Lyse Reagent Kit because it may lead...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: ADVIA Centaur CA 19-9 Assay (250 test kit)-for use Recalled by Siemens...

The Issue: CA 19-9 assay on the ADVIA Centaur CP does not meet the correlation to the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 18, 2016· Spacelabs Healthcare Inc

Recalled Item: Xhibit Central Station Recalled by Spacelabs Healthcare Inc Due to The firm...

The Issue: The firm received reports of telemetry SpO2 numerics dropping off the Xhibit...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Covidien LLC

Recalled Item: Covidien Precision Specimen Container- 4 oz (118 mL) Recalled by Covidien...

The Issue: Sterility of the outer surface of the container compromised due to packaging...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2016· Reshape Medical Inc

Recalled Item: ReShape Integrated Dual Balloon System Recalled by Reshape Medical Inc Due...

The Issue: ReShape Medical is recalling the Integrated Dual Balloon System Gen 1 due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Inlay Optima¿ Multi-Length Ureteral Stent Coated Double Pigtail...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: BARD INLAY Ureteral Stent with Suture Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Bard Fluoro-4 Silicone Ureteral Stent Recalled by C.R. Bard, Inc. Due to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2016· C.R. Bard, Inc.

Recalled Item: Totalis Recalled by C.R. Bard, Inc. Due to Labeling: Statement was added to...

The Issue: Labeling: Statement was added to the Warnings/Precautions section requesting...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Bausch & Lomb, Inc.

Recalled Item: Algerbrush-II Product Usage: Medical - For surgeons to use in Recalled by...

The Issue: According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· Alere San Diego, Inc.

Recalled Item: Alere Triage Total 5 Control Level 1 Recalled by Alere San Diego, Inc. Due...

The Issue: Encoded with incorrect ranges that are not consistent with the ranges...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED OVERSIZED...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED SELF-TAPPING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 12, 2016· DePuy Spine, Inc.

Recalled Item: DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING...

The Issue: SKYLINE Variable Ti screws may have contained SKYLINE Constrained Ti screws...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing