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. 1,090 recalls have been distributed to Virginia in the last 12 months.
Showing 14521–14540 of 53,829 recalls
Recalled Item: Mucus Relief D Recalled by Dr. Reddy's Laboratories, Inc. Due to Subpotent drug
The Issue: Subpotent drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brownie Points Schmurtle 2oz Packaged in food grade cellophane only Recalled...
The Issue: Contains Statement on Label does not include all allergens - Peanuts
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Clobazam Oral Suspension 2.5 mg/mL Recalled by VistaPharm, Inc. Due to...
The Issue: Failed Stability Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) 1 mg/0.5 mg...
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mimvey (estradiol and norethindrone acetate tablets USP) Recalled by Teva...
The Issue: Mislabeling
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NavitrackER Kit A: Knee Recalled by Orthosoft, Inc. dba Zimmer CAS Due to...
The Issue: The product was released for distribution without passing sterilization...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arcos Modular Revision Hip System Recalled by Biomet, Inc. Due to The...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Mini Humeral Stem Recalled by Biomet, Inc. Due...
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Shoulder System Primary Shoulder Stem Recalled by Biomet, Inc....
The Issue: The products in scope underwent an incorrect rework operation for the porous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA SMILE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLEXCERA BASE -a Dental resins for the fabrication of artificial teeth...
The Issue: Manufactured in a non-FDA-registered manufacturing facility and product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer Luer Lok Access Device - intended as a sterile Recalled by...
The Issue: May shed contaminant particles into the urine specimen that may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dole 11 oz Greener Selection / Selection de Verdure Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 3lb Garden Salad SKU: 2163 Recalled by Dole Fresh Vegetables Inc Due to...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dole 16oz Value Size Shredded Lettuce SKU: 157 Recalled by Dole Fresh...
The Issue: Harvest equipment used in harvesting raw iceberg lettuce was tested by Dole...
Recommended Action: Do not consume. Return to store for a refund or discard.