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. 1,800 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,800 in last 12 months

Showing 4064140660 of 51,386 recalls

Medical DeviceFebruary 13, 2015· Medela Inc. EF Division

Recalled Item: - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 Recalled by...

The Issue: The firm is recalling sterile enteral feeding syringes due to determining...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodFebruary 13, 2015· Goya Foods

Recalled Item: Goya Mojo Criollo Marinade for Chicken Recalled by Goya Foods Due to...

The Issue: Goya was notified by one of its ingredient suppliers that one lot of cumin...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 13, 2015· Goya Foods

Recalled Item: Kirby Spanish Barbecue Sauce Mojo Criollo (a) 24 ounce and (c) 1 Gallon...

The Issue: Goya was notified by one of its ingredient suppliers that one lot of cumin...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Apotex Inc.

Recalled Item: Bromfenac Ophthalmic Solution 0.09% Recalled by Apotex Inc. Due to CGMP...

The Issue: CGMP Deviations: Product excipient was not re-tested at the appropriate date.

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

Class III — Low RiskOngoing
Refund
DrugFebruary 12, 2015· Par Pharmaceutical Inc.

Recalled Item: Mafenide Acetate Recalled by Par Pharmaceutical Inc. Due to Presence of...

The Issue: Presence of Foreign Substance; oxidized steel, organic material and shredded...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 12, 2015· Actavis Inc

Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 12, 2015· T. Marzetti Company

Recalled Item: LaRosa's Italian Dressing Recalled by T. Marzetti Company Due to Undeclared...

The Issue: The firm was notified by their customer that the ingredient statement on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodFebruary 12, 2015· T. Marzetti Company

Recalled Item: LaRosa's Creamy Garlic Dressing Recalled by T. Marzetti Company Due to...

The Issue: The firm was notified by their customer that the ingredient statement on...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceFebruary 12, 2015· Stryker Howmedica Osteonics Corp.

Recalled Item: Triathlon Distal Capture Assembly Catalog No: 6541-1-723 The Triathlon...

The Issue: Potential for weld disassociation of the cross pin, which could lead to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda Dual Short Term HygieniKit Milk Collections System (SKU 17115)...

The Issue: Devices were not sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Ameda, Inc.

Recalled Item: Ameda One-Hand Manual Breast Pump (SKU 17161) - Primary packaging Recalled...

The Issue: Devices were not sterilized

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 12, 2015· Dako North America Inc.

Recalled Item: Autostainer Link 48 (AS480) Recalled by Dako North America Inc. Due to A...

The Issue: A false negative result affecting the diagnosis may occur. A defect in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Sybron Dental Specialties

Recalled Item: Outer cardboard box labeling: Pinnacle Cure Sleeve Recalled by Sybron Dental...

The Issue: Cases of Cure Sleeve labeled with part number 4513, which fits 13mm tips,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· Intuitive Surgical, Inc.

Recalled Item: EndoWrist One Vessel Sealer Recalled by Intuitive Surgical, Inc. Due to...

The Issue: Intuitive Surgical has identified the potential for a certain, small portion...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2015· DePuy Orthopaedics, Inc.

Recalled Item: SMARTSET GHV Gentamicin Bone Cement. A self-curing Recalled by DePuy...

The Issue: One lot of SMARTSET GHV Gentamicin Bone Cement is partially agglomerated ....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 11, 2015· Mylan Institutional LLC

Recalled Item: DOXOrubicin Hydrochloride Injection Recalled by Mylan Institutional LLC Due...

The Issue: Correct Labeled Product Mispack: Ifosfamide Injection 50 mg/mL, 60 mL,...

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

Class III — Low RiskOngoing
Refund
FoodFebruary 11, 2015· Sunfood Corportation

Recalled Item: Organic Sacha Inchi Powder Recalled by Sunfood Corportation Due to Sunfood...

The Issue: Sunfood is recalling Sacha Inchi Powder because it has the potential to be...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2015· Tosoh Bioscience, Inc.

Recalled Item: G7 Variant Elution Buffer HiS no. 1 (M) component of Recalled by Tosoh...

The Issue: The G7 Variant Elution Buffer HiS no. 1 (M) is incorrectly labeled with an...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing