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. 2,576 recalls have been distributed to Idaho in the last 12 months.
Showing 9181–9200 of 13,381 recalls
Recalled Item: Atorvastatin Calcium 80 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium 40 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium 20 mg Recalled by Golden State Medical Supply Inc. Due...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...
The Issue: Failed Dissolution Specification: Out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Candesartan Cilexetil Tablets Recalled by Amerisource Health Services Due to...
The Issue: Failed Impurities/Degradation Specifications; 9 month stability (manufacturer)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...
The Issue: Failed Dissolution Specification: Out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Apotex Scientific, Inc Due...
The Issue: Failed Dissolution Specification: Out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metronidazole Injection USP Recalled by Baxter Healthcare Corp. Due to...
The Issue: Presence of Particulate Matter: identified as a cloth fiber.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Presence of Particulate Matter: identified as cardboard.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by Baxter Healthcare Corp. Due...
The Issue: Lack of Assurance of Sterility: potential for leaking containers which lacks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIMIX E 5/15 sulfite-free (5% Amino Acid with Electrolytes in Recalled by...
The Issue: Presence of Particulate Matter: identified as dried skin.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...
The Issue: Failed Dissolution Specifications: Unexplained low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: risperiDONE ORALLY DISINTEGRATING TABLETS Recalled by Zydus Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: Out of specification for a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyrica (pregabalin) capsules Recalled by Pfizer Inc. Due to FAILED...
The Issue: FAILED TABLET/CAPSULE SPECIFICATIONS: Firm is recalling specific lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.