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 1148111500 of 51,386 recalls

Medical DeviceAugust 11, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000 and IMMULITE 2000 XPi Thyroid Stimulating Immunoglobulins...

The Issue: An average negative bias of -23% with IMMULITE 2000/IMMULITE 2000 XPi...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 11, 2022· Exactech, Inc.

Recalled Item: GXL acetabular liners Recalled by Exactech, Inc. Due to Specific GXL...

The Issue: Specific GXL acetabular polyethylene liners, packaged in non-conforming...

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· 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 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· 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
DrugAugust 10, 2022· Family Dollar Stores, Llc.

Recalled Item: Colgate Whitening Mouthwash Recalled by Family Dollar Stores, Llc. Due to...

The Issue: cGMP deviation: Product held outside of appropriate temperature storage...

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

Class II — Potential Health HazardOngoing
Refund
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
DrugAugust 10, 2022· Nephron Sterile Compounding Center LLC

Recalled Item: PF-0.125% Bupivacaine HCl Injection 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
DrugAugust 10, 2022· Nephron Sc Inc

Recalled Item: Ketorolac Tromethamine Injection Recalled by Nephron Sc Inc Due to cGMP...

The Issue: cGMP Deviations: deviations leading to potential cross-contamination.

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

Class II — Potential Health HazardOngoing
Refund