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. 1,099 recalls have been distributed to Kentucky in the last 12 months.

51,386 total recalls
1,099 in last 12 months

Showing 7701–7720 of 28,748 recalls

Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· DeRoyal Industries Inc

Recalled Item: DeRoyal Sterile Custom Kits containing ICU Medical MicroClave Clear...

The Issue: Procedure packs contained a recalled product.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Olympus Corporation of the Americas

Recalled Item: Olympus POWERSEAL 5MM Recalled by Olympus Corporation of the Americas Due to...

The Issue: An out of specification component preventing the blue retention ring from...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to Hip liner...

The Issue: Hip liner implant boxes may contain knee inserts and knee insert boxes may...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 12, 2022· SEDECAL SA

Recalled Item: Sedecal Soltus Battery Mobile X-Ray System 450 Battery Recalled by SEDECAL...

The Issue: Due to un-commanded movement of mobile x-ray unit.

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 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 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 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 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 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