State
73,722 recalls have nationwide distribution and so reach Alabama. 6,377 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,377 recalls naming Alabama we have scored against our rubric, 1,129 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,604 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,377 recalls whose distribution notice names Alabama specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Michigan Herbal Remedies is recalling Tasty Drops CBD oil 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. The product was sold nationwide via internet and retail channels.
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 100 bottles of Pathway To Wellness CBD Oil due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail channels.
Michigan Herbal Remedies is recalling 496 bottles of Made by Hemp 1000MG Hemp Extract due to elevated levels of undeclared lead.
Michigan Herbal Remedies is recalling Tasty Drops Hemp Oil Extract because it 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.
Michigan Herbal Remedies is recalling Javan CBD Oil bottles due to elevated levels of undeclared lead. The product was sold nationwide via internet and retail.
CareFusion is recalling Alaris Auto ID Modules because cleaning agents may damage connectors, causing infusion interruptions and therapy stops.
Michigan Herbal Remedies is recalling 50 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
CareFusion 303, Inc. is recalling 83,532 Alaris PCA Module Model 8120 units because cleaning agents may damage connectors, causing therapy interruptions.
Michigan Herbal Remedies is recalling 25 bottles of BC Hemp Co. CBD Oil due to elevated levels of undeclared lead.
CareFusion 303, Inc. is recalling Alaris System PC Unit Model 8000 infusion pumps because cleaning agents may damage connectors, causing therapy interruptions.
CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because broken platen elements can cause inaccurate fluid delivery, leading to over-infusion, free-flow, or under-infusion.
Yusef Manufacturing Laboratories is recalling Tropical Lip Moisturizer, SPF 30, because the beginning of the batch is approximately 25% superpotent for the active ingredient Meradimate.
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 Hemp Oil Extract due to elevated levels of undeclared lead.
CareFusion 303, Inc. is recalling Alaris Pump Module Model 8100 units because cleaning agents may damage connectors, causing therapy interruptions.
Michigan Herbal Remedies is recalling BC Hemp Co. 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.
Siemens Medical Solutions is recalling 512 Ysio Max X-ray systems due to software issues that may cause collisions or incorrect diagnostic images.
CareFusion 303, Inc. is recalling Alaris Syringe Module Model 8110 units because cleaning agents may damage connectors, potentially interrupting infusion therapy or monitoring.
GE Healthcare is recalling 8,414 CARESCAPE ONE patient monitors because they may fail to provide visual and audible alarms for Ventricular Fibrillation when docked to specific host monitors.
Mylan Institutional LLC is recalling 18,480 vials of Daptomycin for Injection due to the presence of particulate matter. The product is distributed nationwide.