State
73,824 recalls have nationwide distribution and so reach Louisiana. 6,966 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,966 recalls naming Louisiana we have scored against our rubric, 1,107 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,740 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,966 recalls whose distribution notice names Louisiana specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Asher's Chocolate Co is recalling Dark Chocolate Almond Paw products due to potential Salmonella contamination. Consumers should check for Lot # 000336473.
Taro Pharmaceuticals is recalling Nystatin and Triamcinolone Acetonide Cream because it failed content uniformity specifications during 18-month stability testing.
Alcon is voluntarily removing 561,702 Patient Care Kits from the US market because the supplier reported potential sterile packaging compromise.
Smith & Nephew is recalling 100 units of D-RAD orthopedic screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.
Verathon is recalling GVL 2 Stat blades (lot GC32825) because they were physically packaged with the incorrect size device, GVL 1 Stat blades.
Merge Healthcare is recalling Eye Station and Eye Care PACS software because antivirus programs may permanently delete newly captured medical images.
Smith & Nephew is recalling 197 units of D-RAD locking screws because the expiration dates on the labels are incorrect and later than the actual expiration dates.
Smith & Nephew is recalling 19 units of D-RAD locking pegs because the expiration dates on the labels are incorrect and later than the actual dates.
Smith & Nephew is recalling specific Peri-Loc VLP self-tapping cortex screws because the expiration dates printed on the labels are incorrect and later than the actual dates.
Ace Surgical Supply Co., Inc. is recalling 87 INFINITY Internal Hex Healing Abutments because the incorrect device was packaged.
Volkswagen Group of America is recalling 2,091 2015 Audi A3 Cabriolet vehicles because the safety certification label displays an incorrect production date.
Teleflex Medical is recalling Arrow EZ-IO Needle Sets because some individual unit pouches are missing lot numbers and expiration dates.
Valeant Pharmaceuticals is voluntarily recalling 5,647 units of CLENZIderm M.D. Acne Treatment Systems nationwide due to product discoloration.
Valeant Pharmaceuticals is voluntarily recalling CLENZIderm M.D. Pore Therapy Salicylic Acid 2% Acne Treatment due to discoloration.
Grand Design is recalling 2017-2018 Imagine travel trailers because slide room screws may shear, allowing the room to extend while towing and increasing crash risk.
Zutano is recalling about 38,000 infant Cozie booties because the rubber grips on the bottom can detach and pose a choking hazard.
Chrysler is recalling 2014-2017 Ram ProMaster vehicles because labels incorrectly state they have frontal air bags. This mislabeling may increase injury risk in a crash.
Horizon Hobby is recalling specific ECX model vehicles because the electronic speed control can short circuit and catch fire. No injuries or property damage have been reported.
Ducati is recalling 2016-2017 Multistrada 1200 Enduro motorcycles because the rear shock absorber may crack and detach, increasing crash risk.
Nissan is recalling 2016-2017 Titan Crew Cab vehicles because the rear seatbelt assembly may not adequately protect the occupant's head during a crash.
General Motors is recalling 2017 Buick LaCrosse vehicles because incorrectly installed rear suspension toe-links may loosen and disconnect, potentially causing a loss of vehicle control.
National Fleet Services of Ohio is recalling 2016 Ford E-450 vehicles with Roush propane kits because a faulty solenoid may cause the engine to shut off while driving.
Daimler Vans USA is recalling 2013-2014 Freightliner Sprinter and 2016 Mercedes-Benz Metris vehicles because software updates may conflict with vehicle computers, increasing crash risk.
Forest River is recalling 2017-2018 Prime Time Avenger motorhomes because the Federal Placard incorrectly lists tire specifications, potentially leading to improper tire installation.
Riverside RV is recalling 2017-2018 Mt. McKinley and Whitewater travel trailers because they lack required rear-facing reflectors and reflective tail lights, increasing crash risk.