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. 1,891 recalls have been distributed to Virginia in the last 12 months.
Showing 28561–28580 of 53,829 recalls
Recalled Item: SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ Recalled by Smucker...
The Issue: The firm was notified that the product did not have an ingredient panel or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SANTA CRUZ organic CONCORD GRAPE fruit spread NET WT 9.5 Recalled by Smucker...
The Issue: The firm was notified that the product did not have an ingredient panel or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ Recalled by Smucker...
The Issue: The firm was notified that the product did not have an ingredient panel or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Nxtgen Botanicals Recalled by NGB, Corp Due to Potential Salmonella...
The Issue: NGB Corp is recalling Nxtgen Botanicals due to potential Salmonella...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natural Grocers Organic Coconut Smiles Recalled by Natural Grocers by...
The Issue: Coconut smiles product tested positive for Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: SANTA CRUZ organic STRAWBERRY fruit spread NET WT 9.5 OZ Recalled by Smucker...
The Issue: The firm was notified that the product did not have an ingredient panel or...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: diet Pepsi Classic Diet Pepsi Taste Recalled by Pepsico Foods International...
The Issue: PepsiCo is recalling Diet Pepsi due to mislabeling.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Alka-Seltzer Plus¿ packages with a full front panel instant Recalled by...
The Issue: Labeling: Label Mix-Up: Bayer is recalling all Alka-Seltzer Plus packages,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: buPROPion HCl Extended-Release Tablets Recalled by InvaGen Pharmaceuticals,...
The Issue: Failed Dissolution Specifications; during stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rectal Catheters Recalled by Teleflex Medical Europe Ltd Due to These...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: URO-3 Triple Stain (CD44 + p53) with CK20 Recalled by Biocare Medical, LLC...
The Issue: Immunohistochemistry device kits found to display incorrect staining pattern...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a)...
The Issue: These products contain latex, but the following statement is not included on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PHILIPS Xper Flex Cardio Physiomonitoring System Recalled by Invivo...
The Issue: The real-time numeric value for ventricular end-diastolic pressure (EDP)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS Panels¿ CHOL+GLU Test Strips () Recalled by Polymer Technology Systems,...
The Issue: Potential for loss of activity of the glucose analyte (under-recovery) prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect simply InterActive Implant Recalled by Implant Direct Sybron...
The Issue: The cap on the vial might be labeled with the incorrect part number but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision Recalled by...
The Issue: After continuous operation for more than one and a half days, the image on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart (HS1) Onsite/Home AED Recalled by Philips Electronics...
The Issue: An issue with one of the electric components (a resistor) could result in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.