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 1286112880 of 13,398 recalls

DrugJanuary 25, 2013· Hospira Inc.

Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...

The Issue: Non-Sterility: Confirmed customer complaint of product contaminated with mold.

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 23, 2013· Procter & Gamble Hair Care Llc

Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...

The Issue: Cross Contamination with Other Products: Product was mixed with another type...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Mission Pharmacal Co

Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...

The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 23, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....

The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· Fresenius Kabi USA LLC (FK USA)

Recalled Item: IRINOTECAN HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA LLC (FK...

The Issue: Crystallization: Active pharmaceutical ingredient is precipitating in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· RX South LLC DBA RX3 Pharmacy

Recalled Item: Medi-bolic Booster Injectable (methionine 8.3 mg/mL Recalled by RX South LLC...

The Issue: CGMP Deviations: Pharmaceutical for injection was not manufactured according...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 22, 2013· Sandoz Incorporated

Recalled Item: Syeda (drospirenone and ethinyl estradiol) Recalled by Sandoz Incorporated...

The Issue: Tablet/Capsule Imprinted with Wrong ID; a portion of the tablets could...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Rite Aid Maximum Strength Tussin Cough & Cold Mucus Relief CF Recalled by...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Wal-Mart Equate Tussin CF Adult Maximum Strength Recalled by Aaron...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Well at Walgreens Wal-Tussin CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 18, 2013· Aaron Industries Inc

Recalled Item: Select Brand Cough Control CF Max Recalled by Aaron Industries Inc Due to...

The Issue: Presence of Precipitate; white substance confirmed as Guaifenesin, an active...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 17, 2013· Humco Holding Group, Inc

Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...

The Issue: Microbial Contamination of Non-Sterile Product(s): The product has the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2013· Mylan Pharmaceuticals Inc.

Recalled Item: Carvedilol Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Product exceeds specification for...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 11, 2013· AstraZeneca LP

Recalled Item: PULMICORT RESPULES 0.25 mg/2 ml Budesonide Inhalation Suspension (30...

The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 11, 2013· AstraZeneca LP

Recalled Item: PULMICORT RESPULES 0.5 mg/2 ml (30 ampules/carton) Budesonide Inhalation...

The Issue: Does Not Meet Monograph: Budesonide may be slightly above or below the...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 10, 2013· Hospira, Inc.

Recalled Item: Furosemide Injection USP (10 mg/mL) Recalled by Hospira, Inc. Due to Lack of...

The Issue: Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 8, 2013· Hospira Inc.

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

The Issue: Lack of Assurance of Sterility: There is the potential for solution to leak...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 7, 2013· West-ward Pharmaceutical Corp.

Recalled Item: Belladonna Alkaloids (hyoscyamine sulfate Recalled by West-ward...

The Issue: Presence of Foreign Substance: Uncharacteristic blacks spots were found in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 4, 2013· Actavis Pharmaceuticals

Recalled Item: buPROPion Hydrochloride Extended - Release Tablets (XL) 300 mg Recalled by...

The Issue: Failed Dissolution Specifications; 8-hours for the 18-month stability...

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

Class III — Low RiskOngoing
Refund
DrugJanuary 4, 2013· Reumofan Plus USA

Recalled Item: Reumofan Plus Recalled by Reumofan Plus USA Due to Undeclared Active

The Issue: Marketed without an approved NDA/ANDA: Product may contain undeclared active...

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

Class I — Serious Health HazardOngoing
Refund