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. 2,773 recalls have been distributed to Virginia in the last 12 months.
Showing 13301–13320 of 53,829 recalls
Recalled Item: Equate Tartar Control Plus (Eucalyptol 0.092% Recalled by Vi-Jon, LLC Due to...
The Issue: Superpotent Drug: product complaint for milky blue appearance and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arrow Three-Lumen CVC Recalled by ARROW INTERNATIONAL Inc. Due to Gravity...
The Issue: Gravity flow rates on the affected product lidstock are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Battery Recalled by Medtronic Inc Due to Batteries for the HVAD...
The Issue: Batteries for the HVAD system have a weld defect affecting internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tornado Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hilal Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert Recalled by Encore Medical, LP...
The Issue: A right, size 8, knee tibial insert package may include a mispackaged, left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux 200NRe Dialyzer Finished Assy. Recalled by Fresenius Medical Care...
The Issue: Dialyzers were distributed after being exposed to cold temperatures which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK Recalled by...
The Issue: One manufacturing lot is missing the plasma-spray coating in the proximal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sirolimus Oral Solution Recalled by Apotex Corp. Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: Sirolimus Oral Solution recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Keto Living Sugar Control Recalled by Natural Organics, Inc. Due to...
The Issue: Contains undeclared wheat (gluten) in product labeled "gluten free"
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: illumina Model NextSeq 550 Dx Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: illumina Model: MiSeq Dx illumina Model: Recalled by Illumina, Inc. Due to...
The Issue: cybersecurity vulnerability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STORZ KARL STORZ-ENDOSKOPE CMOS Video Cysto-Urethroscope Recalled by Karl...
The Issue: The endoscope may experience a loss of image when activating monopolar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Patient Interface 4.0 (P/N: NIM4CPB1) NIM with Software version...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ratcheting Screwdriver Handle Recalled by Tornier, Inc Due to The device is...
The Issue: The device is unable to meet sterilization requirements when sterilized per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NIM Vital Console 4.0 (P/N: NIM4CM01) NIM with Software version 1.3.2...
The Issue: Software anomaly was identified.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan HCTZ 100/25 mg Recalled by RemedyRepack Inc. Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan HCTZ 100/12.5 mg Recalled by RemedyRepack Inc. Due to CGMP...
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.