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. 1,955 recalls have been distributed to Ohio in the last 12 months.
Showing 20361–20380 of 30,087 recalls
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN SMN 10699533 (500 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device The device is intended for use in Recalled by...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X-Celerator Hydrophilic Exchange Guidewire Catalog No. 103-0601-300...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur¿ Vitamin D Total Assay SMN 10699201 (100 test)...
The Issue: Vitamin D Total- Change in Correlation Between Serum and Plasma Specimen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harmony Insight Diagnostic Monitor Support System - 100 Spring Arm Recalled...
The Issue: The Drager Pendula spring arm device has a set of screws located on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Embolization Device (Pipeline Classic) The device is indicated for...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accessory Adapter Part number 600525A0 Product Usage: designed for the...
The Issue: Maquet Inc. is initiating a voluntary field action on the Accessory Adapter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Marathon Flow Directed Micro Catheter Recalled by Micro Therapeutics Inc,...
The Issue: Delamination and detachment of the PTFE (polytetrafluoroethylene) coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Antibacterial Hydrophilic Intermittent Catheter Recalled by C.R....
The Issue: Misbranding; the product labeled as an Antibacterial Hydrophilic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Guider Softip XF Recalled by Stryker Neurovascular Due to Firm became aware...
The Issue: Firm became aware of potentially defective Guider Guide Catheters due to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.