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 48261–48280 of 53,829 recalls
Recalled Item: Amlodipine Besylate and Benazepril HCl Capsules Recalled by Mylan...
The Issue: CGMP Deviations: Pharmaceuticals were produced and distributed with active...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxycodone and Acetaminophen Tablets Recalled by Watson Laboratories Inc Due...
The Issue: Presence of Foreign Tablets/Capsules: 20 tablets of Oxycodone/APAP 7.5/500...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Recalled by CooperSurgical,...
The Issue: CooperSurgical is recalling two lots of 900-863 because the wrong package...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tri-Nex Healing Abutment Recalled by Southern Implants, Inc Due to Southern...
The Issue: Southern Implants is recalling the Tri-Nex healing abutment because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: pH 7.0 Buffer Solution Pint and Quart Bottles Recalled by Mesa Laboratories,...
The Issue: Mesa Laboratories, Inc. is recalling certain lots of pH 7.0 Buffer Solution...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Performa Angiographic Catheter 5F Multipack. Part numbers...
The Issue: 4 lots of Performa Cardiac Multipacks contain a JR4.0 catheter with a slight...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NX3 Try-In Gel. The product is used as a tooth shade resin material....
The Issue: Kerr Corporation is voluntarily recalling one lot of NX3 Try-In Gel, because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Roasted Salted Mixed Nuts w/ Peanuts Recalled by Dutch Valley Food...
The Issue: Roasted Salted Mixed Nuts with Peanuts were recalled for undeclared tree...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Honey Roasted Peanuts Recalled by Dutch Valley Food Development Inc. Due to...
The Issue: Honey Roasted Peanuts were recalled due to undeclared milk (lactose) and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Access 2 Immunoassay System Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access 2 Immunoassay System because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAQUET Getinge Group CARDIOHELP Base Unit .7999 .8012 Recalled by Maquet...
The Issue: It has come to the attention of MAQUET that in certain rare instances, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Loratadine 24 HR-OTC Recalled by Physicians Total Care, Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Affected lot numbers may contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Risperdal CONSTA (risperiDONE) Recalled by Janssen Pharmaceuticals, Inc. Due...
The Issue: Non-Sterility: Janssen is recalling one lot of Risperdal CONSTA...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Artis zee / zeego Angiography System is designed as Recalled by Siemens...
The Issue: There is a potential issue on running Artis systems running software VC1x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Ceiling Mount MSF-1 for use with M841 and M501 Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Leica Ceiling Mount MS-1F & MC-1F for use with the Recalled by Leica...
The Issue: The ceiling mount supplier encountered an event in which the drive screw in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ******InteGrip ACETABULAR AUGMENT***SMALL 8mm. Use with 48/50mm...
The Issue: Exactech is recalling the InteGrip Acetabular Augments due to an out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Rotoprone therapy System is an advanced patient care system Recalled by...
The Issue: The lock pin can become stuck in the "in" position during the manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PedFuse Bone Probe Recalled by SpineFrontier, Inc. Due to Bone Probes used...
The Issue: Bone Probes used to create a pathway in pedicle bone were manufactured and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Harvest Graft Delivery System Recalled by Harvest Technologies Corporation...
The Issue: Potential for leur connector to leak or have cracks.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.