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. 2,727 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,727 in last 12 months

Showing 1346113480 of 30,087 recalls

Medical DeviceSeptember 16, 2019· KT Health, LLC

Recalled Item: KT RECOVERY+ ICE/HEAT MASSAGE BALL Rolling ball with hot and Recalled by KT...

The Issue: If over-heated may leak which, if not noticed, may cause hot fluid to come...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· CME America, LLC

Recalled Item: BodyGuard Microset Recalled by CME America, LLC Due to When using a specific...

The Issue: When using a specific tubing set with infusion pump system, may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Trocar K-wire 01.6mm x 500mm-Nitinol Product Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Medicrea International

Recalled Item: Medicrea Pass LP Blunt K-wire 01.6mm x 500mm-Nitinol Product : Recalled by...

The Issue: Conical Cannulated Screws may not accept 1.6mm K-Wire, it cannot enter the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Axis-Shield Diagnostics, Ltd.

Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...

The Issue: There is a potential performance issue as detected by an under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Alinity ci Level Sensor Recalled by Abbott Gmbh & Co. KG Due to Potential...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· Abbott Gmbh & Co. KG

Recalled Item: Accessory kit Recalled by Abbott Gmbh & Co. KG Due to Potential reliability...

The Issue: Potential reliability issue with the Alinity ci series Level Sensor, Bulk...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 16, 2019· GE Healthcare, LLC

Recalled Item: CardioLab/ComboLab Recording Systems Recalled by GE Healthcare, LLC Due to...

The Issue: Potential for failure of the patient leakage current test. There is a...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 13, 2019· Draegar Medical Systems, Inc.

Recalled Item: The Infinity Acute Care System (IACS) Monitoring Solution with the Recalled...

The Issue: Cybersecurity vulnerabilities may cause device to reboot, lose alarm...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Merit Medical Systems, Inc.

Recalled Item: Custom Sheath Introducer Kit - Product Usage: intended Recalled by Merit...

The Issue: labeling error: Due to a manufacturing issue, product package was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 12, 2019· Olympus Corporation of the Americas

Recalled Item: Berkeley Disposa-Filter used with Berkeley VC-10 Vacuum Curettage System -...

The Issue: Berkeley Disposa-Filter may possess an insufficient ultrasonic weld defect...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Mizuho America, Inc.

Recalled Item: Microsurgical Operating Room Tables Recalled by Mizuho America, Inc. Due to...

The Issue: Unintended tilting of the Tabletop MST 7300BX and incorrect operation due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Ultrasound Transducer (M1356A) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Loop-Style Tocotransducer (Nautilus) 2264LAX Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Toco MP Transducer (M2734B) Recalled by Pacific Medical Group Inc. Due to...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 11, 2019· Pacific Medical Group Inc.

Recalled Item: Button-Style Ultrasound Transducer (Nautilus) Recalled by Pacific Medical...

The Issue: Fetal/maternal monitor/monitoring systems serviced or remanufactured using...

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

Class II — Potential Health HazardOngoing