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 1150111520 of 51,386 recalls

DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: Trisodium Citrate 0.5% Solution Recalled by Nephron Sterile Compounding...

The Issue: CGMP Deviations: Potential for cross-contamination due to product carryover...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 10, 2022· Angiodynamics, Inc.

Recalled Item: VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog Recalled by...

The Issue: OPS Fiber packaged within specific VenaCure EVLT Procedure Kits does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Steris Corporation Hopkins Facility

Recalled Item: Verify SixCess Challenge Pack. Used to confirm that critical parameters...

The Issue: Product contains incorrect chemical indicators in packaging.

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

Class III — Low RiskOngoing
Medical DeviceAugust 10, 2022· Saranas, Inc.

Recalled Item: Early Bird Bleed Monitoring System Introducer Sheath Set Recalled by...

The Issue: Bleed monitoring system device design error, causing the device to not power...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis icono biplane- Model No. 11327600 Artis icono floor- Model No....

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q floor- Model No. 10848280 Artis Q ceiling- Model Recalled by Siemens...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: Artis pheno- Model No. 10849000 Recalled by Siemens Medical Solutions USA,...

The Issue: Siemens has become aware of a potential hardware issue with Artis Q, Artis...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· DEWEI MEDICAL EQUIPMENT CO LTD

Recalled Item: Dewei DNA/RNA Preservation Kit Recalled by DEWEI MEDICAL EQUIPMENT CO LTD...

The Issue: Products were distributed in the United States without FDA authorization or...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Hologic, Inc

Recalled Item: The BioZorb LP Marker is an implantable radiopaque marker used Recalled by...

The Issue: Hologic BioZorb LP Marker, (Product number F0221), lot number 22A0RL,...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 9, 2022· Baxter Healthcare Corporation

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corporation Due to...

The Issue: Firm noted an increase in customer reports of leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 9, 2022· Technomed Europe

Recalled Item: Disposable Subdermal Needle Electrode Recalled by Technomed Europe Due to...

The Issue: Burns of varying degrees can occur to patients with electrodes left in while...

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

Class II — Potential Health HazardOngoing
DrugAugust 8, 2022· Akorn, Inc

Recalled Item: Timolol Maleate Ophthalmic Solution Recalled by Akorn, Inc Due to...

The Issue: Identification of an unknown impurity at the 12-month stability point....

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

Class III — Low RiskOngoing
Refund
FoodAugust 8, 2022· Yem Foods LLC

Recalled Item: Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) Recalled by Yem Foods...

The Issue: undeclared wheat starch sub-ingredient found in the asafoetida used in the...

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

Class III — Low RiskOngoing
Refund
FoodAugust 8, 2022· Yem Foods LLC

Recalled Item: Priyems Lemon Pickle 1lb/454g Recalled by Yem Foods LLC Due to Undeclared Wheat

The Issue: undeclared wheat starch sub-ingredient found in the asafoetida used in the...

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

Class III — Low RiskOngoing
Refund
FoodAugust 8, 2022· Yem Foods LLC

Recalled Item: Priyems Mango Pickles 1lb/454g Recalled by Yem Foods LLC Due to Undeclared Wheat

The Issue: undeclared wheat starch sub-ingredient found in the asafoetida used in the...

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

Class III — Low RiskOngoing
Refund
FoodAugust 8, 2022· Yem Foods LLC

Recalled Item: Priyems Sambar Coconut & Onion Spicy Lentil Soup 800 grams Recalled by Yem...

The Issue: undeclared wheat starch sub-ingredient found in the asafoetida used in the...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· LNK International, Inc.

Recalled Item: Nighttime Sleep-Aid (doxylamine succinate HCl) tablets Recalled by LNK...

The Issue: Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as...

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

Class III — Low RiskOngoing
Refund
DrugAugust 4, 2022· Baxter Healthcare Corporation

Recalled Item: Acetaminophen Injection Recalled by Baxter Healthcare Corporation Due to...

The Issue: Temperature Abuse: Product distributed in trucks with labels attached to...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 3, 2022· Eclectic Institute Inc

Recalled Item: Eclectic Herb Vitamin Herb Blend vita biotic dietary supplement Recalled by...

The Issue: Product's ingredients names such as Oregon Grape, Cayenne Root, and Ginger...

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 3, 2022· Merit Medical Systems, Inc.

Recalled Item: CorVocet Biopsy System/Catalog Code: CORA1610/B Recalled by Merit Medical...

The Issue: Biopsy Systems have components that are misaligned due to an issue with the...

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

Class II — Potential Health HazardOngoing