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. 1,898 recalls have been distributed to Virginia in the last 12 months.
Showing 28461–28480 of 29,425 recalls
Recalled Item: AmeriWater MRO Dialysis RO+ System Recalled by AmeriWater Inc Due to The...
The Issue: The firm was notified that a malfunction of the device was caused by an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGFA IMPAC CV DICOMStore with Media Purge Daemon (MPD) and Recalled by AGFA...
The Issue: Loss of patient data can occur under certain circumstances due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Devices includes a Multi Port Inflator or without Multi Port Recalled by...
The Issue: Parks Medical Electronics, Inc. was made aware of two incidents where an air...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography (PET) and X-ray Computed Tomography Recalled by...
The Issue: Philips became aware of an issue relating to a UPS battery cabinet that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare conducted...
The Issue: GE Healthcare conducted a recall on various mobile x-ray units (Optima...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur FSH Assay: ADVIA Centaur Calibrator B US: Calibrator Recalled...
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Prolactin Assay: ADVIA Centaur Calibrator B Catalog Number....
The Issue: ADVIA Centaur Prolactin Assay and FSH, Calibrator B fails the analytical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Precise Digital Accelerator Delivery of radiation to defined target volumes...
The Issue: There have been a small number of instances in hospitals where the joint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic...
The Issue: There is a possibility that the ISKD limb lengthener may stop distracting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics Recalled by Stryker Howmedica Osteonics Corp....
The Issue: During the manufacturing of the affected lot a manufacturing error has led...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThyssenKrupp Accessibility LEVANT Stairlift. Intended to mechanically...
The Issue: The seat could break as a result of damage resulting from a seat belt being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare¿ I-Fit" Shower Chair (Models 9780 Recalled by Invacare Corporation...
The Issue: On August 6, 2012, Invacare voluntarily recalled the Invacare¿ I-Fit" Shower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Is-anti-Sm test kits****Catalog No: 720-240*** Product Usage: The...
The Issue: Diamedix Corporation recalled their Is-anti-Sm Test Kit due to the Positive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes(R) Spine Vectra Recalled by Synthes USA HQ, Inc. Due to Although the...
The Issue: Although the reported incidence is low, there is the potential for the drill...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instrumentation Laboratory ACL TOP 500 CTS PN 0000280040 ACL TOP Recalled by...
The Issue: Low Abnormal Fibrinogen Sample Reports as Normal and High Fibrinogen Sample...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Newport HT70 and HT70 Plus Ventilators Recalled by Newport Medical...
The Issue: May emit a continuous high priority alarm and the ventilator may stop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Brivo XR385 DR-F/ X-Ray System X-Ray System Recalled by GE...
The Issue: GE Healthcare has become aware of a software issue on the interface of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Osseotite Tapered Certain Implant 5 X 10mm Model INT510 Biomet Recalled by...
The Issue: Biomet 3i recalled their Osseotite Tapered Certain Implant, Model # INT510...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Brilliance 6 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: The patient support may move in an unintended manner if the foot switch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.