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. 1,029 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,029 in last 12 months

Showing 19481–19500 of 51,386 recalls

Medical DeviceMarch 9, 2020· Boston Scientific

Recalled Item: Stretch VL Ureteral Stent Set 6FX22- 30CM with .035 Sensor UPN:...

The Issue: An increase in the rate of complaints for difficulty or inability to track...

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

Class II — Potential Health HazardOngoing
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 9, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of particulate matter. presence of metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....

The Issue: Presence of foreign substance: Foreign matter has been identified as latex...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars Pineapple Recalled by Dreyers Grand Ice Cream, Inc. Due...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars Strawberry Recalled by Dreyers Grand Ice Cream, Inc. Due...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Dreyers Grand Ice Cream, Inc.

Recalled Item: Outshine Fruit Bars - Variety Pack (contains 24 x 5 oz. units) Strawberry...

The Issue: Firm has received consumer complaints of pieces of white plastic in frozen...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 9, 2020· Coastal Sunbelt Produce Co. Inc.

Recalled Item: Bin Butternut Squash Recalled by Coastal Sunbelt Produce Co. Inc. Due to...

The Issue: Potential Listeria monocytogenes contamination of Butternut Squash

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL29 Recalled by...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A17 Recalled...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Linet Americas

Recalled Item: AVE 2 Birthing Bed - Product Usage: is designated to Recalled by Linet...

The Issue: The UDI on the device label indicates incorrect manufacturer.

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

Class III — Low RiskOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL3 Recalled by...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: ProtekDuo Kit - DL31 RD Recalled by...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemLife Kit Product: 5740-0000...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemLung Kit - DL31 Recalled by...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart pump is assembled into kits: TandemHeart Kit - TS62/A15 Recalled...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 6, 2020· Cardiac Assist, Inc

Recalled Item: TandemHeart Pump Kit Recalled by Cardiac Assist, Inc Due to Failure to prime...

The Issue: Failure to prime due to an assembly error

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

Class II — Potential Health HazardOngoing
DrugMarch 6, 2020· H J Harkins Company Inc dba Pharma Pac

Recalled Item: Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC...

The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 5, 2020· Stonewall Kitchen, LLC

Recalled Item: Stonewall Kitchen Recalled by Stonewall Kitchen, LLC Due to Mislabeling

The Issue: Product is mislabeled as salsa but it contains queso and does not declare...

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

Class II — Potential Health HazardOngoing
Refund