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. 2,790 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
2,790 in last 12 months

Showing 40214040 of 30,087 recalls

Medical DeviceMay 7, 2024· Becton Dickinson & Co.

Recalled Item: BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to Recalled by...

The Issue: Assays may produce false negative results due to decreased activity of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Spine Pack convenience kit Recalled by American...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Hand Pack convenience kit Recalled by American...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Biopsy Drape Pack convenience kit Recalled by...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Laparoscopy Litho Std Pack convenience kit and...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Special Procedure Pack convenience kit Recalled by...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Cataract Pack convenience kit Recalled by American...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Extremity convenience kit Recalled by American...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· American Contract Systems, Inc.

Recalled Item: American Contract Systems Gyn Laparoscopy convenience kit Recalled by...

The Issue: Product released with insufficient aeration time impacting the kits...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· NovaSignal Corp.

Recalled Item: NovaGuide 2 Traditional Ultrasound Recalled by NovaSignal Corp. Due to Due...

The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 6, 2024· NovaSignal Corp.

Recalled Item: NovaGuide 2 Intelligent Ultrasound Recalled by NovaSignal Corp. Due to Due...

The Issue: Due to inadvertently disconnecting grounding cable of ultrasound system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Philips North America Llc

Recalled Item: HA FlexTrak II-Patient transport functionality to transport the patient from...

The Issue: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: ADVANTA VXT Recalled by Atrium Medical Corporation Due to Complaints of...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 3, 2024· Atrium Medical Corporation

Recalled Item: FLIXENE Recalled by Atrium Medical Corporation Due to Complaints of reported...

The Issue: Complaints of reported separation of the Slider GDS Swivel Rod from the...

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

Class II — Potential Health HazardOngoing