Severity 3 of 5
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
Chicago Bar Company LLC is voluntarily recalling RXBAR Pumpkin Spice bars due to undeclared peanut allergen.
Mylan Pharmaceuticals is recalling DrNatura Flora Protect Probiotics because the product contains an undeclared soy allergen.
RXBAR is voluntarily recalling Kids Chocolate Chip bars because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 12-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.
Chicago Bar Company LLC is voluntarily recalling RXBAR KIDS Apple Cinnamon Raisin bars because they contain undeclared peanut.
Chicago Bar Company LLC is voluntarily recalling RXBAR Apple Cinnamon bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
AtriCure is recalling 175 units of the COBRA FUSION 150 Ablation System because patients may face an elevated risk of thromboembolism during specific off-pump procedures.
Chicago Bar Company LLC is voluntarily recalling KIDS Berry Blast bars because they contain undeclared peanut, a major food allergen.
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Chicago Bar Company LLC is voluntarily recalling RXBAR 10-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Mint Chocolate bars due to an undeclared peanut allergen. The recall affects single, 4-count, and 12-count cartons.
Edwards Lifesciences is recalling the Edwards Commander Delivery System due to reports of crimp and inflation balloon component separation during TAVR procedures.
Crate and Barrel is recalling Holiday Bear Acrylic Milk Bottles because the included plastic straw can crack or break, posing a laceration hazard.
Chicago Bar Company LLC is voluntarily recalling RXBAR Coffee Chocolate bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
Chicago Bar Company LLC is voluntarily recalling Coconut Chocolate RXBARs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 14-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
PBM Nutritionals is recalling specific lots of Parent's Choice and Little Journey toddler milk drink powder because the product may contain foreign material.
OMNIlife science Inc. is recalling seven OMNI K1 Broach Handles because the inner pin may become loose and fall out.
Chicago Bar Company LLC is voluntarily recalling RXBAR variety packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Hazelnut bars due to undeclared peanut. Consumers should stop eating these bars.
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.