Product Recalls in Virginia
Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,821 recalls have been distributed to Virginia in the last 12 months.
Showing 5961–5980 of 29,425 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: 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: 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: stryker 3.0MM Neuro Match Head Recalled by Stryker Corporation Due to There...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker 3.0MM Precision Neuro Match Head Recalled by Stryker Corporation Due...
The Issue: There is potential the device inside the package may not match the product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is Recalled by...
The Issue: There is potential the device inside the package may not match the product...
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.
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 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: Legion 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: Medtronic Duet External Drainage and Monitoring system Recalled by Medtronic...
The Issue: Product labeling contains incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.