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. 2,580 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,580 in last 12 months

Showing 2970129720 of 55,415 recalls

FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cranberry Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Raisins Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Pretzel Balls Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Coconut Bites Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Strawberries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Pecans 25 lbs. Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Cherries Recalled by GKI Foods, LLC Due to Undeclared Milk

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
FoodOctober 27, 2017· GKI Foods, LLC

Recalled Item: Dark Chocolate Ginger Snap Cookies Recalled by GKI Foods, LLC Due to...

The Issue: GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2017· Fresenius Kabi USA, LLC

Recalled Item: Midazolam Injection Recalled by Fresenius Kabi USA, LLC Due to Labeling:...

The Issue: Labeling: Label MIX-UP. Blister Packages, Labeled as Midazolam injection,...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) defibrillation electrodes Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 27, 2017· L3 Security & Detection

Recalled Item: L3 Security & Detection System Cabinet X-ray system used for Recalled by L3...

The Issue: L3 has determined in airport environments, there have been several cases...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2017· Physio-Control, Inc.

Recalled Item: LIFEPAK(R) Electrode Starter Kits Recalled by Physio-Control, Inc. Due to...

The Issue: The infant artwork on the product instructs incorrect pad placement. Also,...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· ConvaTec, Inc

Recalled Item: SUR-FIT Natura Moldable Durahesive Skin Barrier with Hydrocolloid Flexible...

The Issue: A portion of Lot 7H02242 outer boxes (market units) of the SUR-FIT Natura...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Arterial Access Tray Recalled by Arrow International Inc Due to The povidone...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2017· Arrow International Inc

Recalled Item: Radial Artery Catheterization Kit Recalled by Arrow International Inc Due to...

The Issue: The povidone iodine prep pads included in certain kits and trays do not meet...

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

Class II — Potential Health HazardOngoing