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. 1,768 recalls have been distributed to Virginia in the last 12 months.
Showing 46521–46540 of 53,829 recalls
Recalled Item: DPM 6 Monitor in use with a Multi Parameter Module Recalled by Mindray DS...
The Issue: The MPM included a cardiac ST/Arrhythmia analysis feature which is not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoll Medical X Series Recalled by ZOLL Medical Corporation Due to...
The Issue: Defibrillator/Pacemaker/Monitor May Latch in a Continuous Device Reset Loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alfa Wassermann Diagnostic Technologies Recalled by Alfa Wassermann, Inc....
The Issue: Extremely low absorbance readings.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fassier-Duval IM Telescopic System. Orthopedic intramedullary rod implant....
The Issue: The outer package label contained the incorrect length of the device. There...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sengstaken Tube and Sengstaken-Blakemore Tube. Teleflex product codes 204800...
The Issue: Sterility of the product cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II Implant Kit with Pocket Controller Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heart Mate II Pocket Controllers removed from packaging Product Usage:...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II LVAD Pump and Pock Controller Kit Recalled by Thoratec...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartMate II System Controller Product Usage: HeartMate II is a Recalled by...
The Issue: Discovery of serious injuries and deaths associated with the process of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zoledronic Acid Injection 5 mg per 100 mL (0.05 mg/mL) Recalled by Sagent...
The Issue: Lack of Assurance of Sterility; leaking of premix bags
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VIVITROL (naltrexone for extended-release injectable suspension) Recalled by...
The Issue: Customer complaints for failure to deliver the dose.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not TABLETS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine Hydrochloride Recalled by McKesson Packaging Services Due to...
The Issue: Failed Dissolution Specification: Out of Specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Quent CAPSULES 4X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Not PORTABLE SIPS Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pleo Quent DROPS 5X Recalled by Terra-Medica Inc. Due to Penicillin Cross...
The Issue: Penicillin Cross Contamination
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.