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. 2,122 recalls have been distributed to Ohio in the last 12 months.
Showing 6001–6020 of 30,087 recalls
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LINK MP Monoblock Hip Stem Recalled by Waldemar Link GmbH & Co. KG (Mfg...
The Issue: Increased force may be required to remove the LINK MP Monoblock trial hip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3D9-3v Transducer Recalled by Philips Ultrasound, Inc. Due to Transducer, an...
The Issue: Transducer, an ultrasound system accessory, consists of two parts that are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeSPARC Pump (part number 5800-0000) contained within TandemLife LifeSPARC...
The Issue: Epoxy used during manufacturing of the LifeSPARC Pump may have uncured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wireless Foot Switch distributed with Philips Allura Xper and Azurion...
The Issue: Loss of availability of the wireless foot switch during procedures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella RP Flex with SmartAssist intracardiac microaxial blood pump Recalled...
The Issue: A higher than expected rate of thrombus formation or deposition has been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Phaco Standalone Tips Recalled by Alcon Research, LTD. Due to Reports of...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT SUV Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSRAIL Platform (Standard Blade) Part Number SB-1000 Recalled by Maquet...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT-i Vacuum Stabilizer System Recalled by Maquet Cardiovascular, LLC...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion FMS Pak Recalled by Alcon Research, LTD. Due to Reports of patient...
The Issue: Reports of patient injury during use in procedures due to potential for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACROBAT V Vacuum Off-Pump System Recalled by Maquet Cardiovascular, LLC Due...
The Issue: The Standard Blade may not securely latch onto the Activator Drive. This may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter Recalled by Covidien LP...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled...
The Issue: Catheter center lumen was found to have an occlusion in the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.