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 1288112900 of 13,398 recalls

DrugJanuary 3, 2013· Mobius Therapeutics LLC

Recalled Item: Mitosol (mitomycin for solution) Recalled by Mobius Therapeutics LLC Due to...

The Issue: Non-Sterility: one or more components of the kit have been found to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2012· Advance Pharmaceutical Inc

Recalled Item: Rugby NATURAL IRON SUPPLEMENT Ferrous Sulfate Recalled by Advance...

The Issue: Labeling; Label Mixup; bottles of Ferrous Sulfate actually contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 28, 2012· Hillyard GMP

Recalled Item: HILLYARD Recalled by Hillyard GMP Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non-Sterile Products: The product may be...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 27, 2012· Ranbaxy Inc.

Recalled Item: Lac-Hydrin (ammonium lactate) Cream Recalled by Ranbaxy Inc. Due to...

The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 27, 2012· Ranbaxy Inc.

Recalled Item: Lac-Hydrin (ammonium lactate) Lotion Recalled by Ranbaxy Inc. Due to...

The Issue: Crystallization: Recall is due to a non-characteristic gritty/sandy texture...

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

Class III — Low RiskOngoing
Refund
DrugDecember 22, 2012· D& S Herbals, LLC

Recalled Item: Super Power capsules Recalled by D& S Herbals, LLC Due to Marketed Without...

The Issue: Marketed Without An Approved NDA/ANDA: This dietary supplement has been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.9 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 21, 2012· Lee Pharmaceuticals, Inc

Recalled Item: 12-Hour Sinus (oxymetazoline hydrochloride) Nasal Spray Recalled by Lee...

The Issue: Microbial Contamination of a Non-Sterile Products: 12-Hour Sinus Nasal Spray...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2012· Warner Chilcott Company LLC

Recalled Item: Femtrace 0.45 mg (Estradiol Acetate) Tablets Recalled by Warner Chilcott...

The Issue: Failed Impurity/Degradation Specifications due to moisture ingress in...

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2012· Matrixx Initiatives Inc

Recalled Item: Zicam Extreme Congestion Relief (oxymetazoline HCl) nasal gel Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Product may be contaminated...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 18, 2012· Belmora LLC

Recalled Item: Flanax (aluminum hydroxide Recalled by Belmora LLC Due to Defective...

The Issue: Defective Container: Product lacks tamper evident breakaway band on cap.

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

Class III — Low RiskOngoing
Refund
DrugDecember 18, 2012· Watson Pharmaceuticals

Recalled Item: Taztia XT(diltiazem HCI extended release capsules Recalled by Watson...

The Issue: Failed Dissolution Specification: Out of a specification result occurred...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· Pacira Pharmaceuticals, Inc.

Recalled Item: EXPAREL (bupivacaine liposome injectable suspension) Recalled by Pacira...

The Issue: Subpotent; bupivacaine

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· L. Perrigo Co.

Recalled Item: Prednisone tablets Recalled by L. Perrigo Co. Due to Presence of Foreign...

The Issue: Presence of Foreign Substance(s); Perrigo has been notified of a recall by...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow XXXTREME Capsules Recalled by Performance Plus Marketing, Inc. Due...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: libigrow capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights SUPREME Capsules Recalled by Performance Plus Marketing, Inc....

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: BLUE Diamond Pill Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: CASANOVA Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 17, 2012· Performance Plus Marketing, Inc.

Recalled Item: Mojo nights Capsules Recalled by Performance Plus Marketing, Inc. Due to...

The Issue: Marketed Without an Approved NDA/ANDA: product may contain undeclared...

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

Class I — Serious Health HazardOngoing
Refund