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. 2,806 recalls have been distributed to Ohio in the last 12 months.
Showing 2081–2100 of 30,087 recalls
Recalled Item: Brand Name: Checkpoint Guardian Intraoperative Lead Product Name: Checkpoint...
The Issue: Adhesive on the back of the lead may not fully encapsulate the metallic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COR Disposable Kit Recalled by DePuy Mitek, Inc., a Johnson & Johnson Co....
The Issue: Device is missing the pin in the graft loader component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medline medical procedure kits, containing Medtronic Aortic Root Cannula
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline medical procedure kits Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Medical convenience kits containing Medtronic Aortic Root Cannula are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Connecta BD Luer-Lok 360 Recalled by BD SWITZERLAND SARL Due to Due to...
The Issue: Due to specific lots of luer-lok devices were shipped to the U.S. market...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix Pillar SA Ti Spacer System Intervertebral Body Fusion Spinal Device...
The Issue: The product is mislabeled with the incorrect anterior height of 10mm, but...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite Inactivated Standard: Inactivated Influenza A/B and Respiratory...
The Issue: The RSV target may give a late Ct value and could potentially not pass QC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Helix Elite" Inactivated Standard: Inactivated SARS-CoV-2 Whole Virus...
The Issue: The A549 human cell target (human cells for sample adequacy control) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) MJ BANDAGE HYDROCOLLOID HEEL OVAL 6CT...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wayson Hydrocolloid Models: 1) Model Number: CUR5103 Recalled by MEDLINE...
The Issue: There is a potential for the sterility of the device to be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CVAC Aspiration System Recalled by Calyxo, Inc. Due to Aspiration system,...
The Issue: Aspiration system, for endoscopic examination/treatment of urinary tract and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MIM software Recalled by MIM Software Inc Due to In situations where two...
The Issue: In situations where two images with differing Fields of View (FOV) complete...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Systems Manager Recalled by CareFusion 303, Inc. Due to Software...
The Issue: Software issue that may result in outdated automated programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Care Coordination Engine (CCE) Infusion Adapter Recalled by CareFusion...
The Issue: Software issue that may result in outdated automated programming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Coated Super Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Initiation 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 18 Coated Regular and 18 Nude Regular Tampons Recalled by DAYE (ANNE'S DAY...
The Issue: Product lacks 510(k) clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.