Product Recalls in Kentucky

Product recalls affecting Kentucky — including food, drugs, consumer products, medical devices, and vehicles distributed to Kentucky. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,609 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,609 in last 12 months

Showing 1302113040 of 13,398 recalls

DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: CVS Pharmacy Fiber Capsules for Regularity Recalled by Raritan...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: DRxChoice Fiber Capsules Recalled by Raritan Pharmaceuticals, Inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Premier Value Fiber Plus Calcium Supplement Capsules Recalled by Raritan...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Up&Up Psyllium Fiber Supplement Recalled by Raritan Pharmaceuticals, Inc....

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Raritan Pharmaceuticals, Inc.

Recalled Item: Simply Right Healthcare Fiber Capsules Recalled by Raritan Pharmaceuticals,...

The Issue: Microbial Contamination of Non-Sterile Products: Product is being recalled...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 4, 2012· Apace KY LLC

Recalled Item: Enalapril Maleate Tablet Recalled by Apace KY LLC Due to Labeling Illegible:...

The Issue: Labeling Illegible: Some bottles labels have incomplete NDC numbers and...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 31, 2012· Hospira Inc.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; product may contain fibrous material

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 29, 2012· Hospira Inc.

Recalled Item: Propofol Injectable Emulsion Recalled by Hospira Inc. Due to Presence of...

The Issue: Presence of Particulate Matter: A single visible particulate was observed...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 29, 2012· Bristol-myers Squibb Company

Recalled Item: BiCNU (Carmustine for injection) 100 mg and Diluent Rx Only Recalled by...

The Issue: Superpotent (Single Ingredient) Drug: All BiCNU lots within expiration which...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Preservative-Free MORPHINE Sulfate Injection Recalled by Hospira Inc. Due to...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· James G. Cole, Inc.

Recalled Item: I-C Drops Recalled by James G. Cole, Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: The product is being recalled because the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 28, 2012· Hospira Inc.

Recalled Item: Diazepam Injection Recalled by Hospira Inc. Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 27, 2012· Samantha Lynn, Inc

Recalled Item: Reumofan Plus Tablets Recalled by Samantha Lynn, Inc Due to Undeclared Drug

The Issue: Marketed without an approved NDA/ANDA: Samantha Lynn Inc. is recalling...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights Recalled by Evol Nutrition Due to Marketed Without an Approved...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Evol Nutrition

Recalled Item: Mojo Nights for Her Recalled by Evol Nutrition Due to Marketed Without an...

The Issue: Marketed Without an Approved NDA/ANDA: The products were found to contain...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 23, 2012· Ferring Pharmaceuticals Inc

Recalled Item: Novarel¿ (Chorionic Gonadotropin for injection Recalled by Ferring...

The Issue: Labeling; incorrect or missing insert; Warnings portion of the Package...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 21, 2012· Ranbaxy Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Ranbaxy Inc. Due to Adulterated...

The Issue: Adulterated Presence of Foreign Tablets: A product complaint was received by...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 15, 2012· Galderma Laboratories, L.P.

Recalled Item: Capex Shampoo (fluocinolone acetonide) Recalled by Galderma Laboratories,...

The Issue: Subpotent; fluocinolone acetonide.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugAugust 15, 2012· Hospira Inc.

Recalled Item: HYDROmorphone HCl Injection Recalled by Hospira Inc. Due to Superpotent...

The Issue: Superpotent (Single Ingredient) Drug: The prefilled cartridge unit has been...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugAugust 14, 2012· Actavis Mid Atlantic LLC

Recalled Item: Prometh VC with Codeine Cough Syrup Recalled by Actavis Mid Atlantic LLC Due...

The Issue: Impurities/Degradation Products: Recalled lots do not meet room temperature...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund