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. 2,731 recalls have been distributed to Ohio in the last 12 months.
Showing 12621–12640 of 30,087 recalls
Recalled Item: Econocare Plus Overlay Item: 1025EC. Intended to aid in the Recalled by...
The Issue: Due to a nonconformance of product contamination (human blood) of Econocare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LabPro Data Management System Recalled by Beckman Coulter Inc. Due to A...
The Issue: A security-only update was released via remote diagnostics on January 14,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo GIA Ultra Universal Stapler 12 mm-intended for resection...
The Issue: Potential for the sterile barrier to be compromised. Products with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SnapLink Recalled by Ormco/Sybronendo Due to The action is being taken due...
The Issue: The action is being taken due to an increase in complaints relating to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COHERENCE Oncologist Recalled by Siemens Medical Solutions USA, Inc Due to A...
The Issue: A potential safety issue arises when an offset calculation is followed by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD Access Systems PowerPort ClearVUE Slim Implantable Port With Smooth...
The Issue: The catheter locks for the lot may contain an 8Fr catheter lock instead of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Hypodermic Safety Needle 30G X 1/2" Item Code 1183005 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject 3mL Syringe with Hypodermic Safety Needle Recalled by Cardinal...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Hypodermic Safety Needle 25G x 5/8" Item Code 1182558 Recalled by...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monoject Bluntfill with Filter Recalled by Cardinal Health 200, LLC Due to...
The Issue: Non-sterile product was shipped to customers. Product package is labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CG4+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT CHEM8+ cartridges (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: The I-STAT BLUE CHEM8+ and CG4+ cartridges are not FDA cleared and do not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epidural Catheterization Kit with FlexTip Plus Recalled by Arrow...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set for Pediatric Lumbar Placement...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.