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. 1,003 recalls have been distributed to Virginia in the last 12 months.
Showing 35561–35580 of 53,829 recalls
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterling Diagnostics Recalled by Sterling Diagnostics, Inc. Due to Sterling...
The Issue: Sterling Diagnostics, Inc. initiated a recall on 7/20/2016 for multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Recalled by...
The Issue: Incorrect drill protocol in the Instructions for Use (IFU)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 16 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core128 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: After upgrading to 3.6.7 software version via FCO72800643, during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva with Flat Detector Recalled by Philips Electronics North...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MultiDiagnost Eleva Recalled by Philips Electronics North America...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Whipknot Soft Tissue Cinch (USP#5) suture. PN: Recalled by...
The Issue: Sterility compromised due to breach in sterile packaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGR Matrix Surgical Mesh Recalled by Novus Scientific Ab Due to Novus...
The Issue: Novus Scientific is implementing additions to the product's instructions for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UroDiagnost Recalled by Philips Electronics North America Corporation Due to...
The Issue: The two bolts that attach the clamping plate to the lateral shaft may break,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...
The Issue: Failed Dissolution Specifications: out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sermorelin 6 mg and Sermorelin 6 mg/GHRP-2 Injection Recalled by Talon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Venlafaxine HCL ER Capsule USP Recalled by Zydus Pharmaceuticals USA Inc Due...
The Issue: Failed Dissolution Specifications: out of specification dissolution results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Human Chorionic Gonadotropin Injection (a) 2500 iu Recalled by Talon...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GFS Honey Roasted Peanuts Recalled by Krispak Inc Due to Undeclared Allergen
The Issue: Krispak, Inc. of Grand Rapids, MI, is recalling a small quantity of Honey...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Original Bacon Flavored Seasoning Salt Recalled by J&D's Down Home...
The Issue: Original Bacon Flavored Seasoning Salt, Big Pig brand, is recalled due to a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bake'n Joy Sanding Sugar Net Wt. 16 lbs. pail Product Number: 0209416...
The Issue: Sanding sugar may contain metal fragments (supplier Domino Sugar)
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BVX-450NR Bovie Precise 360 Handpiece 45cm Recalled by Bovie Medical...
The Issue: The adhesive may be inadequately applied or the assembly may be manipulated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.