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 77817800 of 13,398 recalls

DrugJuly 28, 2017· PD-Rx Pharmaceuticals, Inc.

Recalled Item: Famotidine USP 20 mg Recalled by PD-Rx Pharmaceuticals, Inc. Due to Failed...

The Issue: Failed Tablet/Capsule Specification: out of specification for tablet weight.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· ICU Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection Recalled by ICU Medical Inc Due to Presence...

The Issue: Presence of Particulate Matter; stainless steel

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 26, 2017· HOSPIRA INC, LAKE FOREST

Recalled Item: Hydromorphone Hydrochloride Injection Recalled by HOSPIRA INC, LAKE FOREST...

The Issue: Presence of Particulate Matter: Silicone oil

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 25, 2017· Teva Pharmaceuticals USA

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Teva Pharmaceuticals USA...

The Issue: Failed Impurities/Degradation Specifications: high out of specification...

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

Class III — Low RiskOngoing
Refund
DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health XPLODE 30 capsules Exclusively distribute worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· EZWeightLossTX LLC

Recalled Item: LaBri's Body Health Atomic 60 Capsules Exclusively distributed worldwide by...

The Issue: Marketed Without An Approved NDA/ANDA: Tainted Product Marketed As a Dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 24, 2017· Teva Pharmaceuticals USA

Recalled Item: Famotidine Tablets USP Recalled by Teva Pharmaceuticals USA Due to Failed...

The Issue: Failed Tablet/Capsule Specification; out of specification for tablet weight

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 21, 2017· Chiavna Saffron LLC

Recalled Item: Super Panther 7K Capsules 1250 mg blend Recalled by Chiavna Saffron LLC Due...

The Issue: Marketed without an Approved NDA/ANDA;FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 19, 2017· AVKARE Inc.

Recalled Item: Voriconazole Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed impurities/degradation specifications: Out of specification for a...

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

Class III — Low RiskOngoing
Refund
DrugJuly 17, 2017· BESTHERBS COFFEE LLC

Recalled Item: New Kopi Jantan Tradisional Natural Herbs Coffee Recalled by BESTHERBS...

The Issue: Marketed without an approved NDA/ANDA: presence of undeclared desmethyl...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: ePHEDrine Sulfate 5 mg/mL in NS 5 mL Fill in 12 mL Syringe (25 mg) Recalled...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: morphine sulfate 1 mg per mL in 0.9% Sodium Chloride Recalled by SCA...

The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: MAGNESIUM Sulfate 4 g added to 100 mL 0.9% Sodium Chloride Recalled by SCA...

The Issue: Lack of Assurance of Sterility: Product made with recalled 0.9% sodium...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Hydromorphone 0.5 mg/mL in 0.9% Sodium Chloride 1 mL Fill in 3 mL BD syringe...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 2 mcg/mL + BUPIvacaine 0.1% PF in 0.9% NS 250 mL Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine 50 mg in 0.9% Sodium Chloride 250 mL Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: fentaNYL 10 mcg/mL PF in NS 1 mL Fill in 3 mL syringe Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund