Severity 4 of 5
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.
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.
BMW is recalling hybrid X3, 330e, X5, and 2020 MINI Countryman SE models with loose battery welds that may cause short-circuits and fire. All vehicles have already been remedied.
Faribault Foods is recalling 14-oz. cans of Progresso Organic Chicken Noodle Soup because the product contains undeclared milk, soy, beef, and pork.
Forest River is recalling 2016-2020 Coachmen motorhomes because the awning may deploy while the vehicle is moving, increasing crash risk.
BMW is recalling 2020 X6 and X6 M vehicles because the rear spoiler may not be properly bonded, posing a road hazard risk.
Mercedes-Benz is recalling 2020 GLB 250 vehicles because the rear spoiler may not be welded correctly, posing a road hazard if it detaches.
BMW is recalling specific 2019-2020 motorcycles because front brake calipers may leak fluid, potentially reducing brake performance and increasing crash risk.
Mylan Institutional LLC is recalling 18,480 vials of Daptomycin for Injection due to the presence of particulate matter. The product is distributed nationwide.
Michigan Herbal Remedies is recalling 25 bottles of SP Berry CBD hemp oil because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 25 bottles of 300mg CBD hemp oil because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Goodness Gurus Healthy Hemp Drops due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
Covidien is voluntarily recalling 269 Beacon EUS Access System needles because the cannula detached during procedures in three reported cases.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling A Clean Choice CBD tinctures because they contain elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.
Michigan Herbal Remedies is recalling BC Hemp Co. CBD Oil bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling A Clean Choice CBD Tincture bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 72 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract due to elevated levels of undeclared lead. Consumers should stop using the product.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil bottles due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling 495 bottles of Made by Hemp 1000MG Hemp Extract because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because the product contains elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because the product contains elevated levels of undeclared lead.
Summitt Labs is recalling 236 bottles of KORE Organic CBD Oil Watermelon 15mg due to elevated lead levels. The product was distributed nationwide in the USA.
Covidien is voluntarily recalling 375 units of the Beacon EUS Access System Preloaded Access 90-degree Needle because the cannula may detach during procedures.
Spartan Chemical Co Inc is recalling Lemon Blossom Hand Sanitizer because testing found positive microbial contamination in the product.