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. 2,738 recalls have been distributed to Ohio in the last 12 months.
Showing 11181–11200 of 30,087 recalls
Recalled Item: Bard Conquest PTA Balloon dilation Catheter Recalled by Bard Peripheral...
The Issue: Dilation catheter packaged with the wrong size balloon. The labeling states...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDI Novel Coronavirus COVID-19 IgG ELISA Kit Recalled by Epitope...
The Issue: The use of deionized water rather than distilled water during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COAPTITE Injectable Implant Recalled by Merz North America, Inc. Due to The...
The Issue: The Instructions for Use (IFU) updated 03/02/2020 does not match data listed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products-SARS-CoV-2 IgG Calibrator - Product Usage:...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Monitoring Unit (BMU 40) Recalled by Maquet Cardiovascular Us Sales,...
The Issue: The Printed Circuit Board Assembly (PCBA) are not in compliance with the IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Immunodiagnostic Products Anti-SARS-CoV-2 IgG Control - Product...
The Issue: Elevated sample results signal/cutoff (s/c) values when using eight (8) lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XTANT Medical Recalled by XTANT Medical Due to Cervical Implants contain a...
The Issue: Cervical Implants contain a label that incorrectly identifies the grade of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BladderScan Prime Plus Probe - Product Usage: intended Recalled by Verathon,...
The Issue: Due to a change in handle material and process, probe handle may crack.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 230 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AB PowerCel 170 (velvet black) Recalled by Advanced Bionics, LLC Due to...
The Issue: Mislabeling; It has been determined that some batteries were improperly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien MONOJECT Standard Hypodermic Needle Recalled by Cardinal Health...
The Issue: Potential for the needle to detach from the cartridge after the bottom of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osteosynthesis Compression Staple EasyClip Recalled by Stryker GmbH Due to...
The Issue: The device has the potential to release nickel above the acceptable margin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIDEL Sofia SARS Antigen FIA IVD Recalled by Quidel Corporation Due to Due...
The Issue: Due to false positive results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Platform Fracture Stem Recalled by Exactech, Inc. Due to The device...
The Issue: The device may be incorrectly laser marked as a right stem, when it should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZCA All Poly Acetabular Cup Longevity Crosslinked Polyethylene Recalled by...
The Issue: Sterilant (hydrogen peroxide) used in acetabular cup hip prosthesis...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.