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 10541–10560 of 13,381 recalls
Recalled Item: Fomepizole Injection Recalled by Navinta LLC Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility. A recent FDA inspection reported GMP...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAGNESIUM SULFATE IN 5% DEXTROSE INJECTION Recalled by Hospira Inc. Due to...
The Issue: Labeling: Wrong Bar Code: There is a potential for some units to be...
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 Presence of...
The Issue: Presence of Particulate Matter: Confirmed finding of human hair floating in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% DEXTROSE Injection Recalled by Hospira Inc. Due to Lack of Assurance of...
The Issue: Lack of Assurance of Sterility: there is a potential for solution to leak at...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lamivudine and Zidovudine Tablets USP 150mg/300mg 30 Unit Dose Blisters...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Quinapril Tablets USP Recalled by AVKARE Inc. Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fluticasone Propionate Nasal Spray Recalled by Akorn, Inc. Due to Failed...
The Issue: Failed Stability Specifications: Out of specification for preservative,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxecta(TM) (oxycodone HCl) tablets Recalled by Pfizer Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RIFAMPIN for Injection Recalled by Heritage Pharmaceuticals, Inc. Due to...
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Minivelle (estradiol transdermal system) 0.05 mg/day Recalled by Noven...
The Issue: Temperature Abuse: Prolonged exposure to temperatures outside of labeled...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Colistimethate for Injection USP Recalled by Heritage Pharmaceuticals, Inc....
The Issue: Lack of Assurance of Sterility: Firm is recalling two injectable products...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atracurium Besylate Injection Recalled by Sagent Pharmaceuticals Inc Due to...
The Issue: Lack of Assurance of Sterility: Recall initiated due to FDA observations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PROMETHAZINE DM SYRUP (Promethazine Hydrochloride Recalled by Qualitest...
The Issue: Presence of Foriegn Substance: Plastic cap closure particulates may be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Haloperidol Decanoate Injection Recalled by Mylan Institutional LLC Due to...
The Issue: Lack of Assurance of Sterility; due to leaking vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Inj. Recalled by West-Ward Pharmaceutical Corporation Due...
The Issue: Failed Impurities/Degradation Specifications; 12 month stability testing.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMLODIPINE BESYLATE TABLETS USP Recalled by Qualitest Pharmaceuticals Due to...
The Issue: Failed tablet specifications: One lot was found to contain oversized tablets.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.