State
72,969 recalls have nationwide distribution and so reach Mississippi. 5,349 additional recalls listed Mississippi specifically in their distribution scope.
Of the 5,349 recalls naming Mississippi we have scored against our rubric, 923 (17%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,126 (21%) are Severe.
Which agencies issued them
These figures cover only the 5,349 recalls whose distribution notice names Mississippi specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DEWALT has recalled approximately 17,680 Elite Series 40G T27 High Density Flap Discs because the ceramic cloth abrasive flaps can detach during use, causing laceration and injury. Three reports of the flaps detaching resulted in cuts and scrapes.
Trane U.S. Inc. recalls about 4,790 Gas/Electric Packaged Units because the fuel gas valve can open unexpectedly, causing a gas leak and fire hazard. No injuries have been reported.
NHTSA is recalling 2025 Can-Am Canyon motorcycles because a drive belt support may fail, causing loss of power and increasing crash risk.
Positec is recalling about 49,000 Hyper Tough, Worx, and Portland brand electric corded chainsaws and pole saws due to a defective main switch that can fail and allow the saws to continue running, posing a laceration hazard.
Autocar is recalling 2012-2025 Xspotter vehicles because incorrect tire inflation labels may lead to under-inflated tires, increasing crash risk.
Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.
Teva Pharmaceuticals USA, Inc. is recalling Metoclopramide Tablets, USP 10 mg due to the presence of foreign tablets or capsules in the product. The affected lot is distributed nationwide.
Shyft Group is recalling 2024-2025 Blue ARC BA4L-800 vehicles because a brake caliper spacer may be too big, preventing the parking brake from engaging properly.
Thrive Health Solutions is recalling Semaglutide 2.5 mg/mL pre-filled syringes (Lot #H270221) because the manufacturer cannot assure sterility of the product.
Apotex Corp. is recalling Azelastine Hydrochloride Ophthalmic Solution, USP 0.05% due to lack of assurance of sterility. The affected batch was distributed nationwide.
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices nationwide and internationally because they may contain potentially out-of-specification endotoxin levels and lack sterility assurance.
Thrive Health Solutions is recalling Tirzepatide Injections (10mg/mL, pre-filled syringes) distributed nationwide due to lack of assurance of sterility. Consumers should not use the affected product and contact their healthcare provider.
Thrive Health Solutions is recalling Tirzepatide/Cyanocobalamin Injectable 15mg/1mg/mL pre-filled syringes (Lot C03065F) due to lack of assurance of sterility. The product was distributed nationwide in the USA.
Thrive Health Solutions is recalling NAD+ 100mg/mL pre-filled syringes (Lot #O-O8A01-25) distributed nationwide due to lack of assurance of sterility. Consumers should not use this product.
Bornstein Seafoods Inc. is recalling frozen shrimp meat products after Listeria monocytogenes was detected during the firm's routine testing. The products were distributed nationwide and in Canada.
Thrive Health Solutions is recalling LX Bioboost Plus pre-filled syringes due to lack of assurance of sterility. The affected product is a multi-ingredient injectable formulation distributed nationwide.
Fresenius Medical Care is recalling 0.9% Sodium Chloride Injection in flexible plastic containers nationwide due to lack of assurance of sterility. The FDA classified this as a Class II recall.
Apotex Corp. is recalling Ketorolac Tromethamine Ophthalmic Solution 0.5% due to lack of assurance of sterility. The recall affects 87,840 bottles distributed nationwide.
Integra LifeSciences Corp. is recalling the MicroMyst Applicator Box of 5 due to lack of sterility assurance. The product is used with the Integra Flow Source for controlled application of two liquids.
Integra LifeSciences is recalling Extended Tip Applicator 8CM devices due to potentially out-of-specification endotoxin levels and lack of sterility assurance. The recall affects 6,216 units distributed across the US and internationally.
Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.
Thrive Health Solutions is recalling one lot of Tirzepatide/Cyanocobalamin Injectable pre-filled syringes due to lack of assurance of sterility. The affected product is Lot C03125A distributed nationwide.
Becton Dickinson is recalling BD BACTEC MGIT 960 PZA Kit due to reports of intermittent false resistance results during pyrazinamide susceptibility testing of Mycobacterium tuberculosis. The issue affects units distributed worldwide.
Thrive Health Solutions is recalling Tirzepatide Injections 30mg/mL pre-filled syringes due to lack of assurance of sterility. The affected product was distributed nationwide.
B Braun Medical Inc. is recalling 187,656 containers of 0.9% Sodium Chloride Injection USP due to potential sterility failures caused by pinholes in finger boxes during manufacturing. The defect may allow leaks and compromise the sterile nature of the intravenous medication.