Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. 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 Arkansas in the last 12 months.
Showing 10621–10640 of 13,434 recalls
Recalled Item: Morphine Sulfate Recalled by Pharmedium Services, LLC Due to Presence of...
The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bupivacaine HCl 0.0625% Recalled by Pharmedium Services, LLC Due to Presence...
The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl Recalled by Pharmedium Services, LLC Due to Presence of...
The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLephrine HCl Recalled by Pharmedium Services, LLC Due to Presence of...
The Issue: Presence of Particulate Matter: The firm manufactured products using Hospira...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Erythromycin Pledgets USP Recalled by Akorn, Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Compounded Plaquex Recalled by AnazaoHealth Corporation Due to Good...
The Issue: Good Manufacturing Practices Deviations: The product has an active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BtRiM Max capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EDGE Amplified Weight Release capsules Recalled by Detox Transforms Due to...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNDiGO capsules Recalled by Detox Transforms Due to Undeclared Phenolphthalein
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AMPD GOLD Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: iNSANE Bee Pollen capsules Recalled by Detox Transforms Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nicardipine Hydrochloride Injection Recalled by Mylan Institutional LLC Due...
The Issue: Subpotent Drug and Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KETOROLAC Tromethamine Inj. Recalled by Hospira Inc. Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: 6 month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...
The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
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; Hospira has identified the particulate as a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Recalled by Noven...
The Issue: Defective Delivery System: One lot exceeded the mechanical peel specification
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.