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. 1,047 recalls have been distributed to Idaho in the last 12 months.
Showing 14281–14300 of 48,215 recalls
Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets...
The Issue: Failed Stability Specifications: Out-of-Specification results observed for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methocarbamol 500mg Tablet Recalled by Bryant Ranch Prepack, Inc. dba BRP...
The Issue: Labeling: Label Error on Declared Strength; Bottles labeled as Methocarbamol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irbesartan and Hydrochlorothiazide Tablets USP Recalled by Lupin...
The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AllerClear D-24 hr Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Loratadine-D Extended-Release Tablets (Loratadine and Pseudoephedrine...
The Issue: Failed Moisture Limits
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: CGMP Deviations: Lots recalled because they were manufactured at the same...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...
The Issue: Superpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Medtronic CareLink SmartSync Device Manager application software (D00U005)...
The Issue: The processing of collected episode data may fail due to a software error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Custom Perfusion kits Recalled by Medtronic Perfusion Systems Due...
The Issue: Product is labeled as non-pyrogenic but endotoxin testing was not performed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono biplane with software VE20C-diagnostic imaging angiography...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor with software VE20C-diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis pheno with software VE20C- diagnostic imaging angiography system...
The Issue: Four potential software issues with Artis pheno and Artis icono systems with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioFire Blood Culture Identification 2 (BCID2) Panel Part No: RFIT-ASY-0147...
The Issue: Due to an increased risk of false positive Acinetobacter calcoaceticus-...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.