State
73,737 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,965 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 1,739 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,965 recalls whose distribution notice names Louisiana specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Gillig is recalling 8,224 Low Floor buses because improper circuit breaker ratings may increase the risk of a fire.
Aesculap Implant Systems LLC is recalling specific knee implant components because low-density polyethylene particles may be present on the surface upon opening.
Aesculap Implant Systems LLC is recalling specific knee implant components because low density polyethylene particles may be present on the surface.
Dreyers Grand Ice Cream is recalling Outshine Pineapple Fruit Bars due to consumer complaints of white plastic pieces in the product.
Aesculap Implant Systems LLC is recalling Columbus CR/PS Tibial Plateau knee implant components because low-density polyethylene particles may be present on the surface.
Sun Pharmaceutical Industries is recalling 1,416 bottles of Atorvastatin Calcium 40 mg tablets because a latex glove was found in one lot.
Medtronic is recalling CareLink Encore 29901 programmers due to improper access control and cleartext transmission of sensitive information.
Siemens Healthcare Diagnostics is recalling IMMULITE 1000 Estradiol kits due to high discordant results that may lead to misinterpretation of patient menopausal status.
Aesculap is recalling Columbus R/PS Tibia Plateau knee implant components because low-density polyethylene particles may be present on the surface upon opening.
XTANT Medical is recalling 26 units of OsteoSelect DBM Putty because three devices contained 5.0cc instead of the labeled 10.0cc.
Philips is recalling 534 MultiDiagnost Eleva X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.
Philips is recalling the Velara X-ray generator because a capacitor may fail after electrical surges, preventing image acquisition.
Boston Scientific is recalling four LATITUDE Programming System devices that downloaded unapproved software applications.
Philips is recalling Allura Exper FD Series X-ray generators because a capacitor may fail after electrical surges, preventing image acquisition.
Philips is recalling four UroDiagnost Eleva X-ray systems because a capacitor may fail, preventing image acquisition.
Siemens is recalling Artis Q.zen angiography systems because a software issue could block stand and table movements.
Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.
Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.
Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the production of Solifenacin Tartrate.
Philips is recalling 20 Integris Allura 9 systems because a capacitor may fail, preventing image acquisition.
Philips is recalling 87 Allura Centron X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.
Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.
Philips is recalling 128 Allura CV20 X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.
Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the product converting to Solifenacin Tartrate.
Jubilant Cadista Pharmaceuticals is recalling 89,376 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on tablet edges.