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 1404114060 of 48,215 recalls

FoodNovember 8, 2021· GIVE AND GO

Recalled Item: two-bite unicorn cupcakes 10 oz. Recalled by GIVE AND GO Due to Potential...

The Issue: Potential for metal in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2021· GIVE AND GO

Recalled Item: Favorite Day Bakery Frosted Sugar Cookies 13.5 oz. Recalled by GIVE AND GO...

The Issue: Potential for metal in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodNovember 8, 2021· GIVE AND GO

Recalled Item: two-bite apple caramel cupcakes 10 oz. Recalled by GIVE AND GO Due to...

The Issue: Potential for metal in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 8, 2021· Boston Scientific Corporation

Recalled Item: Boston Scientific ROTAPRO Recalled by Boston Scientific Corporation Due to...

The Issue: Manufacturing instructions did not include the directions to not retest the...

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

Class II — Potential Health HazardOngoing
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 4, 2021· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Flocinolone Acetonide 0.01% Topical Oil Recalled by Amneal Pharmaceuticals...

The Issue: Subpotent Drug: Out-of-specification assay result was obtained for...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· GE Healthcare, LLC

Recalled Item: GE Vscan Extend Recalled by GE Healthcare, LLC Due to The firm identified...

The Issue: The firm identified that the Vscan Extend device will not power on because...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Medtronic Neuromodulation

Recalled Item: Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger...

The Issue: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 4, 2021· Covidien Llc

Recalled Item: Puritan Bennett 980 Series Ventilator Recalled by Covidien Llc Due to...

The Issue: Manufacturing assembly error where a capacitor within the ventilator was...

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

Class I — Serious Health HazardOngoing