State
72,913 recalls have nationwide distribution and so reach Alabama. 6,341 additional recalls listed Alabama specifically in their distribution scope.
Of the 6,341 recalls naming Alabama we have scored against our rubric, 1,121 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,337 (21%) are Severe.
Which agencies issued them
These figures cover only the 6,341 recalls whose distribution notice names Alabama specifically. The 72,913 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Squirrel Brand Travelers Mix in 16 oz cans is being recalled over the potential presence of Salmonella. 3,858 cases are affected.
Ellsworth Sour Cream + Onion Seasoning from PS Seasoning is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
PS Seasoning 1P Original Smokehouse Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 5,375.6 lbs are affected.
UCB Biosciences is recalling CIMZIA (certolizumab pegol) prefilled syringes nationwide because of a lack of assurance of sterility. Affected lots are distributed across the US.
PS Seasoning 1P Jalapeno Heat Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 3,744 lbs are affected.
PS Seasoning & Spices Non Fat Dry Milk in 1 lb packs is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94215T) due to a potential sterile barrier breach. The affected product is a cardiopulmonary bypass vascular catheter distributed worldwide.
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Ember is recalling 2026-2027 Touring Edition trailers because incorrectly tightened shock bolts may detach, creating a road hazard and increasing crash risk.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
Ford is recalling certain 2025-2026 Explorer, Ranger and Bronco vehicles because the engine may fail, resulting in a loss of drive power. 1,536 vehicles are affected.
Ford is recalling certain 2018-2022 Expedition and Lincoln Navigator vehicles because the front seat belt pretensioner may inadvertently lock the belt so it cannot retract or extend.
Becton, Dickinson and Company is recalling Swan-Ganz Pacing Catheter Model D200F7 due to a manufacturing defect that may cause the proximal injectate lumen hub to leak or break, potentially leading to infection, medication loss, or blood loss.
Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.
VitaminAlly Liposomal Women's Liquid Multivitamin Drops, iron free, are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal Women's Liquid Multivitamin Drops with Iron are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
Becton, Dickinson and Company is recalling Swan-Ganz Jr Catheters (models SGPT54, SGPT64P, SGPT755P) because the blue proximal injectate lumen hub may leak or break due to manufacturing changes, risking infection, medication loss, and blood loss.
VitaminAlly Liposomal B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal Sleep Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
VitaminAlly Liposomal Collagen Booster is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.
VitaminAlly Liposomal D3-5000IU Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.