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 1270112720 of 48,215 recalls

Medical DeviceMarch 23, 2022· Sight Sciences, Inc.

Recalled Item: TearCare version 1.0 SmartHubs Recalled by Sight Sciences, Inc. Due to...

The Issue: Ophthalmic devices distributed prior to the recently-obtained 510(k)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 5 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Steris Corporation

Recalled Item: Ultra Pure Non-Woven Sponges Non-Sterile 4-Ply 2 Recalled by Steris...

The Issue: Product not approved for release for US distribution

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Cath Lab Pack Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS Lap Chole Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Spine Pack 2) ACS Lumbar/Back Set Up Tray Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: 1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack Recalled by American...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· American Contract Systems, Inc.

Recalled Item: ACS IR - Angio Pack Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was sterilized with a higher than specification EO concentration.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2022· Microbiologics Inc

Recalled Item: Inactivated macrolide-resistant Mycoplasma genitalium Recalled by...

The Issue: The QC process was not adequate for the specification range.

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

Class II — Potential Health HazardOngoing
DrugMarch 21, 2022· Adamis Pharmaceuticals Corporation

Recalled Item: SYMJEPI (epinephrine injection Recalled by Adamis Pharmaceuticals...

The Issue: Defective Delivery System: Potential clogging of the needle preventing the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Adamis Pharmaceuticals Corporation

Recalled Item: SYMJEPI (epinephrine injection Recalled by Adamis Pharmaceuticals...

The Issue: Defective Delivery System: Potential clogging of the needle preventing the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril and hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Sandoz, Inc

Recalled Item: Orphenadrine Citrate Extended-Release Tablets Recalled by Sandoz, Inc Due to...

The Issue: CGMP Deviations:Nitrosamine impurity (NMOA) above the acceptable daily limit.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril HCl/hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Revive Personal Products Company

Recalled Item: The Natural Dentist Healthy Breath Antiseptic Rinse Recalled by Revive...

The Issue: Labeling; Label mix-up and Wrong Bar Code; back label incorrectly states...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: quinapril HCl/hydrochlorothiazide tablets Recalled by Pfizer Inc. Due to...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 21, 2022· Pfizer Inc.

Recalled Item: Accuretic (quinapril HCl/hydrochlorothiazide) Tablets Recalled by Pfizer...

The Issue: CGMP Deviations: N-nitroso-quinapril and N-nitroso-hydrochlorothiazide...

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

Class II — Potential Health HazardOngoing
Refund