Product Recalls in Ohio

Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,790 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,790 in last 12 months

Showing 38613880 of 30,087 recalls

Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Vertix Solitaire - The Vertix MD Trauma has been Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM MULTIX MT - Intended Radiographic X ray Table is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2024· Siemens Medical Solutions USA, Inc

Recalled Item: ZE for Vertix Solitaire - The AXIOM Vertix Solitaire is Recalled by Siemens...

The Issue: Short circuit in the power supply unit (PSU) of the Touch Display may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Single Patient Use (SPU) Circuit 5kit for Volara Recalled by...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Baxter Healthcare Corporation

Recalled Item: Volara System. Blue Ventilator Adapter Module. Intermittent positive...

The Issue: Potential of the handset plug to disconnect from the nebulizer port on the...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Scaler Tip - Perio Model/Catalog Number: 261669 The scaler Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2024· Dental EZ Group Star Dental Division

Recalled Item: Titan Blis-Sonic Scaler packaged with the Titan Scaler Tip - Recalled by...

The Issue: Tip holder portion of the scaler tip assembly may have an oversized...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Cardinal Health 200, LLC

Recalled Item: Presource kits and trays Recalled by Cardinal Health 200, LLC Due to...

The Issue: Cardinal Health is following the FDA's recommendations regarding the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Integra LifeSciences Corp.

Recalled Item: CUSA Excel C2600 23KHz Straight Handpiece-Indicated for use in surgical...

The Issue: Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 29, 2024· Baxter Healthcare Corporation

Recalled Item: Life2000 Ventilator Recalled by Baxter Healthcare Corporation Due to...

The Issue: Potential for certain Life2000 ventilator systems to either fail to charge...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch Recalled...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 28, 2024· Artivion, Inc

Recalled Item: CryoValve SG Pulmonary Human Heart Valve Recalled by Artivion, Inc Due to...

The Issue: Grafts were found to have been approved, released, shipped and implanted...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-FR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-V Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Hitachi America, Ltd., Particle Therapy Division

Recalled Item: Brand Name: PROBEAT Product Name: PROBEAT-CR Model/Catalog Number: N/A...

The Issue: During positioning within the system's 3D to 3D matching mode while...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2024· Beckman Coulter Inc.

Recalled Item: Beckman Coulter Recalled by Beckman Coulter Inc. Due to LIH Influence check...

The Issue: LIH Influence check settings for Lipemia are incorrect which may result...

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

Class II — Potential Health HazardOngoing