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. 2,641 recalls have been distributed to Arkansas in the last 12 months.
Showing 4581–4600 of 13,434 recalls
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to Product...
The Issue: Product Mix-Up: a complaint received indicating mix-up of 10 mg Lisinopril...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Presence of Particulate Matter - found in reserve sample vials at the firm.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Recalled by...
The Issue: Labeling: Not elsewhere classified: Observed separation in the secondary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ceftazidime for Injection USP and Dextrose for Injection USP Recalled by B....
The Issue: Failed Stability Specifications: Out-of-Specification (OOS) results for High...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefixime for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...
The Issue: Subpotent Drug: low out of specification (OOS) test result observed in long...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nizatidine Oral Solution Recalled by Amneal Pharmaceuticals of New York, LLC...
The Issue: CGMP Deviations: potential N-Nitrosodimethylamine (NDMA) amounts above...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KORE ORGANIC CBD Oil Watermelon 15mg* Recalled by Summitt Labs Due to...
The Issue: Chemical Contamination; product contains elevated levels of lead
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estradiol Recalled by B & B Pharmaceuticals, Inc. Due to Foreign Object...
The Issue: cGMP deviations: Presence of foreign material (Teflon)introduced at the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Finasteride Plus 1.25 mg Capsule Recalled by MasterPharm LLC Due to Cross...
The Issue: Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets Recalled by Golden State Medical Supply Inc. Due...
The Issue: CGMP Deviations: Impurity for N-nitroso-N-methyl-4-aminobutryric Acid (NBMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lisinopril Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to...
The Issue: Presence of Foreign Tablet/ Capsule: Product complaint received indicating...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 30 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 20 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 100 mg Recalled by Avet Pharmaceuticals, Inc....
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tablets USP 50 mg Recalled by Avet Pharmaceuticals, Inc....
The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Injection Recalled by Akorn Inc Due to Failed...
The Issue: Failed impurities/degradation specification: Out-of-Specification result for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.