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. 1,067 recalls have been distributed to Virginia in the last 12 months.
Showing 17661–17680 of 53,829 recalls
Recalled Item: Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible...
The Issue: The affected Milex Gellhorn pessaries were incorrectly manufactured with a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OT1000 Series Orthopedic Surgical Tables Recalled by Steris Corporation Due...
The Issue: On January 7, 2021, STERIS identified that the glued bond between the beam...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oseltamivir Phosphate for Oral Suspension Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications; Out-of-specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidocaine/Tetracaine (LIPO110)* 23%/7% Ointment 100 GMS per 4 ounce plastic...
The Issue: Superpotent Drug. Lidocaine higher concentration than listed
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Door County Coffee & Tea Co. French Vanilla Flavored Cappuccino. Recalled by...
The Issue: Retail Box did not contain list of ingredients or allergen statement.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HOUSE AUTRY TARTAR SAUCE NET WT 9 OZ (255g) DISTSRIBUTED BY House -Autry...
The Issue: The firm received a consumer complaints that the product was spoiled.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Captivator II Single-Use Polypectomy Snares Outer box UPN Recalled by Boston...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator Single-Use Polypectomy Snares Recalled by Boston Scientific...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSpan Transseptal Needles Catalog No. FND-019-01 Recalled by Merit...
The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartspan Transseptal Needles Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The labeled needle tip curvature of specific lots of transseptal needles may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM...
The Issue: Distributed COVID test kits without emergency use authorization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions Ethicon Endo-Surgery Recalled by Stryker...
The Issue: Product was distributed without receiving regulatory clearance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various reprocessed products: PROVISION Recalled by ReNovo, Inc. Due to...
The Issue: Non-sterile product was shipped to customers labelled as sterile.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares...
The Issue: Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tube Tracheostomy and Tube Cuff Recalled by Smiths Medical ASD Inc. Due to...
The Issue: Smiths Medical became aware that three lot numbers of a specific model of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Central Screw 6.5x25mm - Product Usage: used as a sterile Recalled by...
The Issue: Zimmer Biomet is conducting a lot specific medical device recall for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConMed 50L abdominal insufflator Recalled by Northgate Technologies, Inc....
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Steris CO2MPACT Endoscopic Insufflator system Recalled by Northgate...
The Issue: An internal tubing component in the flow path was made with incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CervAlign Anterior Cervical Plate System-Cervalign Recalled by RTI Surgical,...
The Issue: Locking mechanism has been observed to disassociate either intraoperatively...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.