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. 2,544 recalls have been distributed to Idaho in the last 12 months.

48,215 total recalls
2,544 in last 12 months

Showing 1278112800 of 48,215 recalls

Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 5V RT ADULT Model: 32028781 50604-US...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode - IP SET 6V RT ADULT-US Model: 32028780...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 15, 2022· Graphic Controls Acquisition Corporation

Recalled Item: CLARAVUE Pre-wired Electrode IP-SET N3 - PEDIATRIC-US Model: 32028776...

The Issue: Instructions for Use (IFU) (Instructions for Use) indicate compliance with...

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

Class II — Potential Health HazardOngoing
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: TETRACAINE 1% Tetracaine HCI Injection Recalled by Vitae Enim Vitae...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PHENOBARBITAL Sodium Injection Recalled by Vitae Enim Vitae Scientific, Inc....

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Vitae Enim Vitae Scientific, Inc.

Recalled Item: PAPAVERINE HYDROCHLORIDE Injection Recalled by Vitae Enim Vitae Scientific,...

The Issue: Lack of Assurance of Sterility: deviations from Current Good Manufacturing...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection 50 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Epinephrine Injection 8 mg per 250 mL in 0.9% Sodium Chloride Recalled by...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 8 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 16 mg per 250 mL added to Recalled by...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection in 0.9% Sodium Chloride Recalled by Athenex...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Phenylephrine HCl Injection 40 mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMarch 14, 2022· Athenex Pharma Solutions, LLC

Recalled Item: Norepinephrine Bitartrate Injection 4mg per 250 mL in 0.9% Sodium Chloride...

The Issue: Defective container

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 14, 2022· Neuralynx Inc

Recalled Item: ATLAS Stim Headbox-NK For use only with the ATLAS Neurophysiology Recalled...

The Issue: Atlas Stim Headbox (ASHB) was delivered to US customers under a premise that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 14, 2022· Sensory Medical Inc

Recalled Item: Cub 2 Enclosed Bed Canopy System Recalled by Sensory Medical Inc Due to Due...

The Issue: Due potential misuse of the product, firm is updating warnings and...

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

Class I — Serious Health HazardOngoing
DrugMarch 11, 2022· DASH Pharmaceuticals LLC

Recalled Item: Sucralfate Oral Suspension Recalled by DASH Pharmaceuticals LLC Due to...

The Issue: Labeling: Label Mix-Up

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 11, 2022· DePuy Orthopaedics, Inc.

Recalled Item: VELYS Robotic-Assisted Solution Base Product No.: 451570100 Recalled by...

The Issue: System software v1.5.1 has a system software issue related to the Daylight...

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

Class II — Potential Health HazardOngoing