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. 2,592 recalls have been distributed to Ohio in the last 12 months.
Showing 23861–23880 of 55,415 recalls
Recalled Item: ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Recalled by...
The Issue: Mixer blade may separate from mixer due to the screw and nut failure and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dragonfly Dehydrate Guava Ing: Guava Recalled by U.S. Tov, Inc. Due to...
The Issue: Undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac ECTR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject" 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook/Triangle Blade Kit Recalled by Stryker GmbH Due to The...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 201 Vet Pak Hypodermic Needle Recalled by Cardinal Health 200, LLC...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Item code: 8881200029 Recalled by...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Standard Hypodermic Needle Recalled by Cardinal Health 200, LLC Due...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Blunt Cannula Recalled by Cardinal Health 200, LLC Due to...
The Issue: Manufacturing defect was found for the cartridge component, which could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.