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 2776127780 of 55,415 recalls

FoodJune 8, 2018· Caito Foods Service, Inc.

Recalled Item: Multiple Brands Mixed Melon: Customer Product Description Pack Weight...

The Issue: Products have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 8, 2018· Caito Foods Service, Inc.

Recalled Item: Multiple Brands Mixed Melon: Customer Product Description Pack Weight...

The Issue: Products have the potential to be contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodJune 8, 2018· Golden Star Wholesale Inc

Recalled Item: Al Reef dried apricot sour Recalled by Golden Star Wholesale Inc Due to...

The Issue: Golden Star Wholesale, Inc. initiated a voluntary recall of Al Reef dried...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Stryker Neurovascular

Recalled Item: Synchro2 Recalled by Stryker Neurovascular Due to The product labels (pouch...

The Issue: The product labels (pouch and carton) for products contain an incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect Recalled by Bio-Rad Laboratories, Inc Due to Abnormal coloration...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Bio-Rad Laboratories, Inc

Recalled Item: MRSASelect II Recalled by Bio-Rad Laboratories, Inc Due to Abnormal...

The Issue: Abnormal coloration of agar plates and the growth of non-characteristic MRSA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 8, 2018· Zimmer Surgical Inc

Recalled Item: Zimmer Dermatone AN Recalled by Zimmer Surgical Inc Due to Devices may have...

The Issue: Devices may have a loose control bar, which could compromise the ability to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2018· GE Medical Systems, LLC

Recalled Item: GE Healthcare MRI Systems Recalled by GE Medical Systems, LLC Due to The...

The Issue: The latest on-site software version may not have been reinstalled at some...

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

Class II — Potential Health HazardOngoing
DrugJune 6, 2018· Pharmalucence, Inc.

Recalled Item: Kit for the Preparation of Technetium Tc99m Medronate Recalled by...

The Issue: Lack of assurance of sterility: Technetium TC-99M Medronate Kit has a...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2018· GE Medical Systems, LLC

Recalled Item: Discovery MR750w Nuclear Magnetic Resonance Imaging System labeled as the...

The Issue: GE Medical Systems has discovered a small area on the bore surface of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2018· Tosoh Bioscience Inc

Recalled Item: G8 Automated HPLC Analyzer: HLC-723G8-ST Recalled by Tosoh Bioscience Inc...

The Issue: HbAE is known to interfere with the HbA1c assay on the current version of...

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

Class II — Potential Health HazardOngoing