These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Extract Labs recalled 19,720 Elderberry gummies on August 26, 2025 due to potential peanut protein cross-contact. The gummies, containing 20mg CBD and 20mg D9 THC each, were shipped unlabeled in bulk packaging. Consumers should not consume these products and seek refunds or replacements.
B. Braun Medical Inc. recalled 26,316 bags of Sterile Water for Injection on August 26, 2025. The recall affects the 3000 mL product due to potential fluid leakage from a misaligned port. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Extract Labs recalled 19,750 gummies on August 26, 2025, due to potential peanut protein cross-contact. The products, which contain 20mg of CBD and 20mg of D9 THC per gummy, lack proper labeling. Consumers should not consume these gummies and should contact the company for refunds or replacements.
Extract Labs recalled 2,180 bottles of sugar-free mixed berry gummies on August 26, 2025. The recall stems from potential peanut protein cross-contact, posing a risk to consumers with allergies. The gummies contain 10mg of CBD and 10mg of D9 THC per serving.
Extract Labs recalled 19,810 units of Blue Razz 20mg Gummies on August 26, 2025. The recall follows concerns about potential peanut protein cross-contact. Consumers should not consume the product and should seek a refund.
W L Gore & Associates recalled over 52,000 vascular grafts on August 26, 2025, due to reports of delamination. The defect can lead to severe complications such as bleeding or cannulation difficulties. Affected products include multiple model numbers, which were distributed across the United States and internationally.
Country Eggs, LLC recalled 81,542 dozen shell eggs on August 26, 2025. The eggs may be contaminated with salmonella, posing a serious health risk. Consumers should not eat these products.
Abdallah Candies recalled one box of Cream Caramels on August 25, 2025. The product contains undeclared allergens, specifically peanuts and pecans. This poses a serious risk to consumers with nut allergies.
Abdallah Candies recalled Sea Salt Caramel Dark Miniature on August 25, 2025. The recall affects one 5.20 lb box due to undeclared allergens. Consumers should not consume the product and seek a refund immediately.
AvKare recalled 1,512 cartons of Chlorpromazine Hydrochloride Tablets on August 25, 2025. The recall follows the discovery of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from healthcare providers.
TopCare Health recalled 60 bottles of 70% Isopropyl Alcohol on August 25, 2025. The recall stems from cross-contamination with other products. Consumers should stop using the product immediately.
AvKare recalled 2,003 cartons of Chlorpromazine Hydrochloride Tablets on August 25, 2025. The recall stems from the presence of a foreign substance in the medication. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Kroger recalled 1,860 cans of 70% Isopropyl Alcohol on August 25, 2025. The recall resulted from cross contamination with other products. Consumers should stop using the product immediately and seek guidance from healthcare providers.
LeMaitre Vascular recalled 10 Artegraft Collagen Vascular Grafts on August 25, 2025, due to incorrect labeling. The devices lack CE and UKCA marks and are missing essential patient information. No distribution occurred within the U.S., but the affected products were sent to Great Britain and Switzerland.
Ultra Violette recalled 49,275 tubes of its Velvet Screen SPF 50 sunscreen on August 22, 2025. Testing revealed SPF levels inconsistent with the label, posing a serious risk. Consumers should stop using the product immediately.
CooperVision recalled 180 units of Sofmed Breathables contact lenses on August 22, 2025. The recall affects one lot manufactured with an invalid sterilization cycle. Patients and healthcare providers must stop using the affected lenses immediately.
Ultra Violette recalled 44,497 tubes of its Mini SPF Mates kit on August 22, 2025. The sunscreen products showed inconsistent SPF results, including readings as low as SPF 4. Consumers must stop use immediately and contact the distributor for guidance.
CooperVision recalled 90 units of Voyant 1-Day Premium Toric contact lenses on August 22, 2025. The recall affects one lot manufactured with an invalid sterilization cycle. Consumers should stop using the product immediately and follow recall instructions.
CooperVision recalled 4,140 units of MyDay Toric contact lenses on August 22, 2025, due to an invalid sterilization cycle. The recall affects lenses distributed nationwide, particularly in Florida, Kentucky, North Carolina, and Wisconsin. Users must stop using these lenses immediately to avoid potential health risks.
GE Medical Systems recalled 29,225 units of the MAC VU360 Acquisition Trunk Cable and Module Holder on August 22, 2025. Users may incorrectly place the Acquisition Module, leading to cable damage and potential overheating. Affected devices were distributed globally, including the U.S. and several other countries.