Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,617 recalls have been distributed to Mississippi in the last 12 months.
Showing 10681–10700 of 13,570 recalls
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: 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: 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: 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: 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: 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.
Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...
The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...
The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.