Recalls
Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.
Minimum severity
Ford is recalling certain 2025-2026 Bronco and Bronco Sport vehicles because the instrument panel cluster may fail at startup, preventing drivers from seeing warning lights and vehicle speed.
Diva Fam Inc is recalling Sea Moss Gel Superfood nationwide due to potential Clostridium botulinum contamination. No illnesses have been reported.
Beacon Promotions Inc is recalling repackaged M&Ms candies (Item BB458BG) because they contain undeclared milk, soy, and peanut allergens. Consumers with allergies to these ingredients are at risk.
Diva Fam Inc is recalling Sea Moss Gel Superfood products nationwide due to potential Clostridium botulinum contamination. Consumers should discard the product and stop using it.
Diva Fam Inc is recalling Sea Moss Gel Superfood nationwide due to potential Clostridium botulinum contamination. The product was distributed through retail and online channels.
Imu-Tek Immuno-5 Colostrum Powder 7 oz (Lot #216) is being recalled due to undeclared milk allergen. Consumers with milk allergies should not consume this product.
Diva Fam Inc is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination. The product is distributed nationwide; consumers should not consume affected units.
Diva Fam Inc is recalling Sea Moss Gel Superfood due to potential Clostridium botulinum contamination. Consumers should not consume the affected product and should return it to the place of purchase.
Diva Fam Inc is recalling Sea Moss Gel Superfood Pineapple nationwide due to potential Clostridium botulinum contamination. Consumers should not consume the product.
Willy Pete's Chocolates Almond Despair is recalled because almonds are not declared in the ingredient statement, posing a risk to consumers with tree nut allergies. The product was distributed in Massachusetts, South Carolina, and Connecticut.
Diva Fam Inc is recalling cherry-flavored sea moss gel due to potential Clostridium botulinum contamination. The product was distributed nationwide through retail and online channels.
Diva Fam Inc is recalling Sea Moss Gel Superfood (16 FL OZ jars) due to potential Clostridium botulinum contamination. The product is distributed nationwide.
Prima Foods International voluntarily recalled BarbaCuban Cubama White Truffle Sauce because the product contains undeclared quinine. The recall affects 12,214 bottles distributed in Florida.
Sea Moss Gel Superfood (Lemon Pie flavor) is being recalled due to potential Clostridium botulinum contamination. The product was distributed nationwide through retail and online channels.
Beacon Promotions Inc is recalling repackaged M&Ms Peanut candies (1.3 oz) due to undeclared milk, soy, and peanut allergens. The affected lot (M1823200) was distributed across 19 states.
BarbaCuban 90 Miles to Mojo Marinade distributed in Florida is recalled due to undeclared quinine. Prima Foods International voluntarily recalled 12,214 bottles of the product.
Diva Fam Inc is recalling Sea Moss Gel Superfood (strawberry, 16 FL OZ) due to potential Clostridium botulinum contamination. The product is distributed nationwide through retail and online sales.
Olympus Corporation is recalling Single Use 3-Lumen Sphincterotome V devices (Model KD-VC411Q-0320) because some units did not undergo proper thermoforming and could deform or lose performance during use.
Olympus is recalling CleverCut Single Use 3-Lumen Sphincterotomes (Model KD-V411M-0320) because some units may not have undergone proper thermoforming, potentially causing device deformation and performance loss.
Olympus is recalling Single Use 3-Lumen Sphincterotome V instruments (Model KD-V411M-3020) because some devices may not have undergone proper thermoforming, causing potential deformation and performance loss. The recall affects 650 units.
Olympus Corporation is recalling approximately 2,344 Single Use 3-Lumen Sphincterotome V devices due to manufacturing defects that could cause deformation and loss of surgical performance.
Vortex Surgical is recalling surgical backflush needles due to voids in Tyvek pouch seals that compromise the sterile barrier. The defect could allow bioburden contamination leading to infection risk.
A software timing issue in MiniMed 780G insulin pumps (software version 6.60) may trigger pump errors that suspend insulin delivery. 577 units are affected, distributed in the US and Israel.
Olympus is recalling over 17,600 3-Lumen Sphincterotome V devices because some units did not undergo proper thermoforming, which could cause them to deform and lose performance.
VANTIVE US HEALTHCARE is recalling 115,112 PRISMAFLEX HF1000 dialyzer sets nationwide due to potential dislodgement of the deaeration chamber from the control unit.