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. 2,570 recalls have been distributed to Idaho in the last 12 months.
Showing 10461–10480 of 13,381 recalls
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Lack of...
The Issue: Lack of Sterility Assurance: The product has the potential to leak at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydroxyzine Hydrochloride Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Olanzapine Recalled by Apotex Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Acarbose Tablets 50 mg a)10 x 10 Unit Dose Tablets per Blister Pack Recalled...
The Issue: Subpotent Drug: The firm received an out of specification result for Assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: C-Topical 4% CII (cocaine hydrochloride) Recalled by Cody Laboratories, Inc....
The Issue: Labeling: Label mix-up; bottles were incorrectly labeled as 10 mL instead of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine Hydrochloride Tablets Recalled by Mylan Institutional, Inc....
The Issue: Failed Impurities/Degradation Specifications: the manufacturer, recalled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cartia XT (diltiazem HCl extended-release capsules Recalled by Actavis...
The Issue: Presence of Foreign Substance; fine residue or dust identified as aluminum...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GLIPIZIDE and METFORMIN HYDROCHLORIDE Tablets Recalled by Heritage...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROMETHAZINE VC WITH CODEINE SYRUP Recalled by Qualitest Pharmaceuticals Due...
The Issue: Failed Impurities/Degradation Specifications: A stability lot was out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Rose Bengal GloStrips (rose bengal) Ophthalmic Strips USP Recalled by Nomax...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluorescein Sodium Ophthalmic Strips USP Recalled by Nomax Inc Due to Failed...
The Issue: Failed Content Uniformity Specifications: The product may not meet finished...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp Due to...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gemcitabine for Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clinimix E 5/20 sulfite-free (5% amino-acid with electrolytes in 20%...
The Issue: Lack of Assurance of Sterility; increased complaints received for leaks
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.