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. 2,727 recalls have been distributed to Ohio in the last 12 months.
Showing 13401–13420 of 30,087 recalls
Recalled Item: Aesculap Sterile disposable fleece drape Recalled by Aesculap Implant...
The Issue: Packaging seal integrity not validated resulting in a lack of sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Hard Base Implantable Port with Attachable 9.6 F Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. X-Port isp M.R.I Implantable Port Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerFlow Implatable Apheresis IV Port with attachable 9.6 F ChronoFl...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort M.R.I. Implantable Port with Attachale 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BardPort Titanium Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Power Port isp M.R.I. Implantable Port with Attachable 9.6 Recalled by...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.PowerPort Implantable Port With Attachable 9.6 F Open-Ended Single-Lumen...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Vaccess CT Power-Injectable Implantable Port with Suture Plugs Recalled...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. PowerPort M.R.I. Implantable Port with Attachable 9.6 F Open-Ended...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1. Groshong 9.5 Dual-Lumen CV Catheter Recalled by Bard Peripheral Vascular...
The Issue: Firm has identified that the product may be at risk of incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Low Profile Screw Recalled by Arthrex, Inc. Due to Screws provided in the...
The Issue: Screws provided in the device package are 6 mm longer than intended.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accutorr 3 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosebud Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rosie4 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accutorr 7 Vital Signs Monitor with NIBP valve assembly board Recalled by...
The Issue: NIBP valve assembly board subject to this recall includes enhancements that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Glucose Monitoring System Recalled by Roche Diabetes Care, Inc. Due to...
The Issue: Potential power issues with the Accu-Chek¿ Guide Blood Glucose Monitoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.