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. 2,634 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
2,634 in last 12 months

Showing 78617880 of 13,398 recalls

DrugJune 28, 2017· Valeant Pharmaceuticals North America LLC

Recalled Item: Obagi-C Rx System C-Therapy Night Cream Recalled by Valeant Pharmaceuticals...

The Issue: Labeling: Incorrect or Missing Package Insert - Obagi-C Rx System C-Therapy...

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

Class III — Low RiskOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 20 mMol in Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection 15 mMol in Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 5% Dextrose Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Potassium PHOSphate in 0.9% Sodium Chloride Injection Recalled by PharMedium...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2017· PharMedium Services, Llc

Recalled Item: Succinylcholine Chloride Injection (Preserved) 20 mg per mL Recalled by...

The Issue: Lack of Assurance of Sterility; media fill failure at manufacturer

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Curcumin Emulsion 10mg/ml Injection Recalled by ImprimisRx CA, Inc., dba...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Latanoprost PF Solution Recalled by ImprimisRx CA, Inc., dba ImprimisRx Due...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Latanoprost PF Solution (0.5-0.005)% Recalled by ImprimisRx CA,...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 23, 2017· ImprimisRx CA, Inc., dba ImprimisRx

Recalled Item: Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic...

The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Advanced Pharma Inc.

Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2017· Vitility

Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class I — Serious Health HazardOngoing
Refund