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. 2,694 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,694 in last 12 months

Showing 1408114100 of 55,415 recalls

Medical DeviceFebruary 11, 2022· Huntleigh Healthcare Ltd.

Recalled Item: HUNTLEIGH Disposable intraoperative Probe Recalled by Huntleigh Healthcare...

The Issue: Faceplate may become detached from the probe body.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2022· RaySearch America Inc

Recalled Item: RayStation 4-11B Recalled by RaySearch America Inc Due to Incorrect source...

The Issue: Incorrect source to skin or surface distance (SSD) calculation may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 11, 2022· Abbott Molecular, Inc.

Recalled Item: Alinity m Integrated Reaction Units (IRU) Recalled by Abbott Molecular, Inc....

The Issue: There is potential for the Reaction Vessels (RVs) detaching from the RV cap...

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

Class II — Potential Health HazardOngoing
DrugFebruary 10, 2022· Positive Health

Recalled Item: RISE UP RED EDITION Capsules Recalled by Positive Health Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
FoodFebruary 10, 2022· Ardent Mills, LLC

Recalled Item: Ardent Mills Hotel and Restaurant All Purpose Flour - AA Recalled by Ardent...

The Issue: Raw, untreated flour tested positive for Salmonella.

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

Class II — Potential Health HazardOngoing
Refund
FoodFebruary 10, 2022· J & M Foods, Inc.

Recalled Item: Favorite Day Carrot cake soft bake cookies Net Wt 8 Recalled by J & M Foods,...

The Issue: Pecans although listed in the Ingredient Statement, was omitted from the...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System Driver SKU: NX-DR Orthopedic surgical...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 3.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle 3.2 Proximal Kit SKU: Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 10, 2022· Nextremity Solutions

Recalled Item: Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Recalled...

The Issue: Proximal end of the driver is oversized in varying degrees, making it...

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

Class II — Potential Health HazardOngoing
DrugFebruary 9, 2022· Walmart Stores

Recalled Item: Avaphinal Maximum Male Enhancement Sexual Pills Recalled by Walmart Stores...

The Issue: Marketed Without An Approved NDA/ANDA: Product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 9, 2022· Lannett Company, Inc.

Recalled Item: Diazepam Oral Solution (Concentrate) Recalled by Lannett Company, Inc. Due...

The Issue: Failed Impurities/Degradation Specifications: Out of specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 9, 2022· bioMerieux, Inc.

Recalled Item: VIDAS CMV IgM Recalled by bioMerieux, Inc. Due to Invalid calibrations (out...

The Issue: Invalid calibrations (out of range high) while using the product.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Fructosamine (Fruc) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Lithium_2 (LITH_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H) Recalled by Siemens...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica CH Calcium_2 (CA_2) Recalled by Siemens Healthcare Diagnostics,...

The Issue: Siemens Healthcare Diagnostics Inc. has confirmed the potential for reagent...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2022· Maquet Cardiovascular, LLC

Recalled Item: Ultima Activator II Reusable Drive Mechanism Recalled by Maquet...

The Issue: Potential for corrosion on the pins of the Ultima Activator II Reusable...

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

Class II — Potential Health HazardOngoing
DrugFebruary 8, 2022· ABC Sales 1 Inc

Recalled Item: MAC DADDY RED Capsules Recalled by ABC Sales 1 Inc Due to Undeclared Tadalafil

The Issue: Marketed Without An Approved NDA/ANDA: product was found to contain...

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

Class I — Serious Health HazardOngoing
Refund