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. 2,813 recalls have been distributed to Virginia in the last 12 months.
Showing 6681–6700 of 29,425 recalls
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft Recalled...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft Recalled by...
The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT PS #4 13MM Intended for Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRIATHLON X3 TIBIAL BEARING INSERT CS #3 12MM-Intended for knee Recalled by...
The Issue: Mislabeled:Labeled Catalog Number: 5531-G-312-E, TRIATHLON X3 TIBIAL BEARING...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Teleflex (manufacturer: Vascular SOLUTIONS) D-Stat Flowable Hemostat...
The Issue: The product contains an expired diluent vial. If the impacted product is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultraview SL (UVSL) Command Module Recalled by Spacelabs Healthcare, Inc....
The Issue: Command modules will display the following when parameter processing is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation Cranial Software Recalled by Medtronic Navigation, Inc. Due...
The Issue: During non-axial/some axial exams, software anomalies occur during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Mission Disposable Core Biopsy Instrument Kit: Recalled by Bard...
The Issue: Coaxial cannula internal diameter and length of biopsy instruments exceed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henry Schein Hard Line Chairside Reline kit-Resilient Acrylic Denture...
The Issue: The Hard Line Chairside Reline Kit (570-0718) (0921940HS) was labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Over-Head Ceiling Tube Support Recalled by SHIMADZU CORPORATION MEDICAL...
The Issue: Eight fixing bolts at the base of the X-ray ceiling tube column assembly may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reliance Vision Multi-Chamber Washer/Disinfector Recalled by Steris...
The Issue: In the remote occurrence in which the electrical contactor component present...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: stryker ORTHOLOC 3Di Fusion Plate MTP Right Recalled by Wright Medical...
The Issue: Two lots of Ortholoc 3Di Fusion plates contain incorrect dorsiflexion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cytrellis ellacor System with Micro-Coring Technology-Dermal Micro-Coring...
The Issue: Irregular core patterns could cause potential overlap of cores at the 8%...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray Recalled by...
The Issue: There were reports from customers that the tracheostomy in the sets and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set Recalled by...
The Issue: There were reports from customers that the tracheostomy in the sets and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metal Tray Recalled by Karl Storz Endoscopy Due to Metal sterilization trays...
The Issue: Metal sterilization trays used to encase and protect medical devices during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity Image-Guided Radiation Therapy System containing an MR gradient...
The Issue: There is a low possibility that an electrical connector in the MR gradient...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.