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. 1,146 recalls have been distributed to Ohio in the last 12 months.

55,415 total recalls
1,146 in last 12 months

Showing 8081–8100 of 30,087 recalls

Medical DeviceJune 22, 2022· ASO LLC

Recalled Item: (1) CVS Health Sterile Surgical Pads Recalled by ASO LLC Due to The product...

The Issue: The product falls apart during handling after removal from its primary...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethemet cables are missing one or both ferrite cores therefore the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2022· Touch US Llc

Recalled Item: etouchus Recalled by Touch US Llc Due to Device was marketed without FDA...

The Issue: Device was marketed without FDA 510(k) clearance or a PMA.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 20, 2022· Bard Access Systems, Inc.

Recalled Item: Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit...

The Issue: BD Intraosseous Needle Kits may exhibit: 1) Increased force required to...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 17, 2022· Luminex Corporation

Recalled Item: Verigene CDF Nucleic Acid Test Recalled by Luminex Corporation Due to There...

The Issue: There is a potential for false negative results using VERIGENE CDF Stool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin.net model MN5000 Software Recalled by St. Jude Medical, Cardiac...

The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2022· Luminex Corporation

Recalled Item: VERIGENE Enteric Pathogens Nucleic Acid Test Recalled by Luminex Corporation...

The Issue: There is a potential for false negative results using VERIGENE CDF Stool...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin 2 PCS MER37000 programmer Model MER3400 software Recalled by St. Jude...

The Issue: The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 17, 2022· St. Jude Medical, Cardiac Rhythm Management Division

Recalled Item: Merlin PCS 3650 programmer Model 3330 software Recalled by St. Jude Medical,...

The Issue: There is a potential for programmer software (Merlin PCS) and remote...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: AquaC UNO H [120V Recalled by Fresenius Medical Care Holdings, Inc. Due to...

The Issue: Internal ethernet cable may be misaligned, the cable jacket (insulation)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Breast Abdominoplasty Pack Recalled by American Contract Systems, Inc. Due...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various convenience packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Cysto Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Angiography packs/trays Recalled by American Contract Systems, Inc....

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Angiography/Cath Lab packs/trays Recalled by American Contract...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various ENT Packs Recalled by American Contract Systems, Inc. Due to Product...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· NordicNeuroLab AS

Recalled Item: nordicBrainEX Recalled by NordicNeuroLab AS Due to When exporting merged...

The Issue: When exporting merged results from the BOLD, DSC, and DCE modules of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various Pacemaker Packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 16, 2022· American Contract Systems, Inc.

Recalled Item: Various neurology packs Recalled by American Contract Systems, Inc. Due to...

The Issue: Product was exposed to multiple sterilization cycles without validation for...

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

Class II — Potential Health HazardOngoing