State
73,388 recalls have nationwide distribution and so reach Alabama. 6,371 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,371 recalls naming Alabama we have scored against our rubric, 1,131 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,602 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,371 recalls whose distribution notice names Alabama specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Renaissance Food Group is recalling Tri-Pepper Blend (7 oz units) due to positive test results for Listeria monocytogenes. All products manufactured with the same components are included in the recall.
Renaissance Food Group is recalling Spicy Guacamole Blender products because positive test results confirmed Listeria monocytogenes contamination in the finished product.
Renaissance Food Group is recalling Hatch Chile Guacamole Blender due to positive test results for Listeria monocytogenes. Products were distributed to Alabama, Georgia, and South Carolina.
Renaissance Food Group is recalling Diced Red Onion (10 oz units) distributed to Alabama, Georgia, and South Carolina due to positive test results for Listeria monocytogenes in finished product.
Renaissance Food Group is recalling diced bell pepper and white onion products due to positive test results for L. monocytogenes. The recalled products were distributed in Alabama, Georgia, and South Carolina.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
Eden's Answers Inc is recalling Sprigs Lil Ones Sleepy Time herbal supplement due to high bacterial growth in the product. Consumers should stop using it immediately.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
WFM 365 Organic Creamy Caesar dressing is recalled because the product does not declare wheat and soy allergens on its label. Consumers with wheat or soy allergies should not consume this product.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Philips has recalled MR Patient Care Portal 5000 desktop units (Model 453564792561) due to intermittent audio failure. The device may fail to produce audio, and standard troubleshooting does not reliably resolve the issue.
Eden's Answers Inc is recalling Sprigs Dental Health, an herbal dietary supplement, due to detection of high bacterial growth. The product was distributed across 37 states.
Eden's Answers Inc is recalling Sprigs Honey Herbal Syrup dietary supplement due to high bacterial growth within the product. The affected product was distributed across multiple states.
Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.
AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.
FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.
Kia is recalling certain 2021-2023 K5 and 2021-2022 Sorento vehicles with transmission oil pump malfunction that may cause complete loss of drive power, increasing crash risk.
Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.
Chrysler is recalling specific Mopar brake hoses because the inside diameter may be too small, causing rupture and loss of braking ability.