Virginia recalls
3,571 federal recalls affecting Virginia in the last 12 months - 209 Virginia-specific plus 3,362 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideCheck your AXIOS Stent lot number immediately
Boston Scientific's AXIOS Stent (a medical device used in certain procedures) may fail to deploy or expand properly during use. If the stent does not expand as intended, patients may need additional procedures—either endoscopic or surgical—to remove the stent and repair the site.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideContact your doctor about AXIOS Stent
Boston Scientific is recalling certain AXIOS Stents (8mm x 8mm) due to reports of deployment and expansion problems during use. If a stent fails to deploy properly, patients may need additional procedures to remove it and repair the puncture site.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideCheck HOT AXIOS Stent lot numbers immediately
Boston Scientific's HOT AXIOS Stent (6mm × 8mm) may fail to deploy or expand properly during placement. If the stent does not expand correctly, patients may need additional endoscopic or surgical procedures to remove it and repair the puncture site.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideContact your doctor about Boston Scientific AXIOS Stent
Boston Scientific is recalling certain AXIOS Stents (8mm x 8mm) used in medical procedures because they may not deploy or expand properly. If the stent fails to deploy correctly, additional procedures may be needed to remove it and repair the puncture site.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideContact your doctor about AXIOS Stent recall
Boston Scientific has recalled certain AXIOS Stents (6mm x 8mm) due to reports of problems with stent deployment and expansion during procedures. In some cases, the stent may not deploy properly, potentially requiring additional procedures to remove it and repair the site. No injuries have been reported.
- 2026-02-11FDA-DeviceBoston ScientificClass INationwideStop using Boston Scientific AXIOS Stent
Boston Scientific has recalled specific lots of the AXIOS Stent and Electrocautery-Enhanced Delivery System (20mm x 10mm) due to reports of stent deployment and expansion problems. In some cases, the stent may not deploy or expand properly, which could require additional procedures to remove the stent and repair the puncture site.
- 2026-02-11FDA-FoodB.C. Williams Bakery ServiceClass INationwideStop using B.C. Williams Swiss Chocolate Cake Mix
B.C. Williams Bakery Service, Inc. is recalling Swiss Chocolate Cake Mix because it contains milk that is not listed on the label. This poses a serious risk to anyone with a milk allergy. The affected product was distributed nationwide in 50 lb. bags with lot codes 072925-220 and 071825-36.
- 2026-02-11FDA-FoodB.C. Williams Bakery ServiceClass INationwideStop using B.C. Williams Bakery Bread and Roll Mix
B.C. Williams Bakery Service, Inc. is recalling Bread and Roll Mix in 50 lb. bags because they may contain milk that is not listed on the label. This poses a serious risk to people with milk allergies. The affected product was distributed nationwide.
- 2026-02-11FDA-FoodB.C. Williams Bakery ServiceClass INationwideStop using B.C. Williams Spice Cake Mix
B.C. Williams Bakery Service, Inc. recalled Spice Cake Mix (50 lb. bags, Batch 221) because it contains milk that is not listed on the label. This poses a serious risk to people with milk allergies or severe lactose intolerance. The recall affects 51 bags distributed nationwide.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's orange Sea Moss Gel Superfood (16 FL OZ glass jars) may be contaminated with Clostridium botulinum, a bacteria that can cause botulism, a serious illness affecting the nervous system. The recall affects specific lot codes distributed nationwide and sold online.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's Lemon Pie Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacteria that can cause serious illness. The product was sold nationwide through retailers and online. No injuries have been reported so far.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc is recalling its 16 FL OZ Soursop Sea Moss Gel Superfood due to potential contamination with Clostridium botulinum, a bacteria that can cause serious food poisoning. The affected product was sold nationwide through retail stores and online. No illnesses have been reported to date.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc is recalling its Sea Moss Gel Superfood (16 FL OZ glass jars) due to potential contamination with Clostridium botulinum, a bacteria that can cause botulism, a serious illness affecting the nervous system. The affected product was sold nationwide through retail stores and online.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's Sea Moss Gel Superfood in Mango and Pineapple flavor may be contaminated with Clostridium botulinum, a bacteria that produces a dangerous toxin. The affected product was sold nationwide through retailers and online. No illnesses have been reported yet.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's Cherry-flavored Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The product was sold nationwide through retail stores and online. No illnesses have been reported to date.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam strawberry sea moss gel
Diva Fam Inc's strawberry-flavored Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The product was sold nationwide through retailers and online. No illnesses have been reported so far.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Sea Moss Gel Superfood in Blue Spirulina and Raspberry flavor may be contaminated with Clostridium botulinum, a bacteria that produces a dangerous toxin. The contamination was discovered during testing. No illnesses have been reported so far.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc is recalling Passion Fruit-flavored Sea Moss Gel Superfood (16 FL OZ glass jars) because it may be contaminated with Clostridium botulinum, a bacteria that produces a dangerous toxin. The affected product was sold nationwide through retail stores and online.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc is recalling Elderberry Sea Moss Gel Superfood due to potential contamination with Clostridium botulinum, a bacterium that can cause serious illness. The affected 16 FL OZ glass jars were sold nationwide through retail stores and online.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's Apple and Cinnamon Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The affected 16 FL OZ glass jars were distributed nationwide through retail stores and online sales. No illnesses have been reported so far.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam sea moss gel
Diva Fam Inc's Wildcrafted Sea Moss Gel Superfood may be contaminated with Clostridium botulinum, a bacterium that produces a dangerous toxin. The affected product is sold nationwide in glass jars (16 fl oz) with specific lot codes. No illnesses have been reported so far.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam Sea Moss Gel Superfood
Diva Fam Inc's pineapple-flavored Sea Moss Gel Superfood may contain Clostridium botulinum, a bacteria that produces a toxin causing botulism, a serious illness. The contamination affects multiple lot codes distributed nationwide and sold online.
- 2026-02-11FDA-FoodDiva FamClass IINationwideStop using Diva Fam mango sea moss gel
Diva Fam Inc is recalling mango-flavored Sea Moss Gel Superfood due to potential contamination with Clostridium botulinum, a bacterium that can cause serious illness. The affected product was sold nationwide in 16 fl oz glass jars through retail stores and online.
- 2026-02-11FDA-FoodBeacon PromotionsClass IIRepackaged M&Ms candies, Net Wt 1.3 oz. Item BB458BG. Labeled with the following promotional company names. 1. Next Up, 2. Smith Pro, 3. Jaxport, Jacksonville Port Authority, 4. Climax Molybdenum, A Freeport-McMoRan Company, 5. University of Maryland, School of Public Policy, 6. Liberty University Environmental Health & Safety, 7. Subaru, 8. Trinity Cyb3r, 9. Candy Treats, 10. JSE, Jordan & Skala Engineers, 11. Dropbox DocSend, 12. PP, Prosperity Promotions, 1
Undeclared allergens (milk, soy, and peanut)
- 2026-02-11FDA-FoodBeacon PromotionsClass IIStop eating Make Your Mark M&Ms candy
Beacon Promotions Inc repackaged M&Ms Peanut candies (1.3 oz, Item BB471BG, labeled "Make Your Mark") contain undeclared allergens: milk, soy, and peanut. The affected lot is M1823200 with best-by date 4/30/2026. These candies were distributed across 20 states.
- 2026-02-11FDA-FoodOptiwizeClass IIINationwideStop using OptiWize Collagen Plus
OptiWize Inc. recalled OptiWize Collagen Plus (320 count bottles) after testing found the manganese level was lower than stated on the label. The company discovered that labeled ingredient quantities did not match the actual amounts in the product.
- 2026-02-11FDA-FoodFazt & LoudClass IIINationwideStop drinking Fazt & Loud Lost and Found Energy
Fazt & Loud LLC is recalling Lost and Found Energy Sour Gummy Bear drinks because the label says each can has 150mg of caffeine, but they actually contain 300mg—twice as much. This mislabeling affects 16oz cans from lot MO-00911 with a best-by date of 11/13/2027 distributed nationwide.
- 2026-02-11FDA-DrugSun PharmaceuticalClass IINationwideStop using Sun Pharmaceutical Diclofenac Sodium Gel
Sun Pharmaceutical is recalling one lot of Diclofenac Sodium Topical Gel, 3% (Lot #AD92721, expiring 3/31/2027) because the gel's thickness is slightly lower than required specifications. The product was distributed nationwide and is sold by prescription only.
- 2026-02-11FDA-DrugGranulesClass IINationwideStop using Granules trazodone 50 mg
Granules Pharmaceuticals is recalling certain bottles of trazodone 50 mg because some bottles may contain foreign tablets or capsules mixed in. This affects 71,424 bottles with batch number 6160008A and an expiration date of 12/31/2026. No injuries have been reported.
- 2026-02-11FDA-DrugGreen LumberClass INationwideStop using Green Lumber Natural Fuel For Men
Green Lumber Natural Fuel For Men capsules were sold as a supplement but contain tadalafil, a prescription medication approved only for treating erectile dysfunction and certain heart conditions. The product was marketed and sold without FDA approval and without listing tadalafil on the label. Tadalafil can cause serious side effects, especially in people taking certain other medications or with certain health conditions.
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