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. 1,026 recalls have been distributed to Virginia in the last 12 months.
Showing 27721–27740 of 53,829 recalls
Recalled Item: MAGnesium 4gm in NS 100 mL (MAGnesium SULfate (USP) 4 gm Recalled by Avella...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL 3 mcg/mL Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 50 mg Recalled by Avella of...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MORphine 1 mg/mL (Morphine Sulfate Recalled by Avella of Deer Valley, Inc....
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.2% ROPivacaine Recalled by Avella of Deer Valley, Inc. Store 38 Due to...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: fentaNYL (10 mcg per mL) in 0.95 Sodium Chloride Recalled by Avella of Deer...
The Issue: Lack of Assurance of Sterility: Potential leakage of bags.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Teleflex MEDICAL Pilling(R) UNIVERSAL SHEARS 7 1/2" Recalled by Teleflex...
The Issue: The incorrect plastic was used to manufacture the handles of these shears,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive...
The Issue: Incorrect use-by date on the device registration/patient file labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics, Inc. Due to In 2018, Philips...
The Issue: In 2018, Philips Respironics added foam replacement to the preventive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monsel's Solution (Ferric Subsulfate) Recalled by BioDiagnostic...
The Issue: CGMP Deviations: Products not manufactured under current good manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lyfetrition Live Life Nutritiously Vitamin B12 2 FL. OZ bottle Recalled by...
The Issue: The firm was informed that the product did not contain vitamin B12...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Alpha Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Gamma Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Express Fluid Warmer (FW-300 Recalled by NxStage Medical, Inc. Due...
The Issue: There is a potential risk of electrical fire when fluid leaks into the power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nokia BPM+ Wireless Blood Pressure Monitor Product System Recalled by...
The Issue: Device could not meet the requirements for systolic pressure
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve with Pulse Wave Cassette Recalled by Cardinal Health...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MyLab Seven Recalled by ESAOTE S.P.A. Due to The probe power monitoring...
The Issue: The probe power monitoring settings have been found to be not appropriate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydroline Trumpet Valve Recalled by Cardinal Health 200, LLC Due to The...
The Issue: The suction valve may not close properly which could cause continuous suction.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.