State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.
Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.
Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.
Becton Dickinson & Company is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Stryker is recalling T4 Zipper Toga sterile personal protection garments because material layers may separate, creating a risk of exposure to contaminants.
Zimmer Biomet is recalling 19,483 Pressure Sentinel Intramedullary Reaming System Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Integra LifeSciences is recalling 250 units of the TCC-EZ Total Contact Cast System because a quarantined lot may produce excessive heat.
Maharaja Food Importers is recalling frozen MMRF Neyyappam because the label lists ghee but fails to declare milk, a major allergen.
Maharaja Food Importers is recalling frozen MMRF Kumbiliappam because the label lists ghee but fails to declare milk as an ingredient.
Coastal Meds, LLC. is recalling 4,524 vials of Methylcobalamin Injectable due to the presence of unknown particulate matter.
Sofradim Production is recalling Versatex Monofilament Mesh due to patient reports of abdominal hernia recurrence following repair. The firm has updated instructions to warn surgeons about risks in specific procedures.
Stryker is recalling T5 Zipper Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Coastal Meds, LLC. is recalling 1,309 vials of LIPO-DEN Injectable-30 mL because of the presence of unknown particulate matter.
Winnebago is recalling 293 recreational vehicles because roof racks may detach due to incorrect fasteners, creating a road hazard.
Stryker is recalling T4 Pullover Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Stryker is recalling T5 Zipper Toga sterile garments because material layers may separate, posing a risk of exposure to contaminants.
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires due to potential failure of the sterile packaging seal.
Zimmer Biomet is recalling 19,483 Natural Nail System Tear Drop Guide Wires due to a potential failure of the sterile packaging seal.
FDA is recalling EEA Hemorrhoid and Prolapse Stapler Sets due to a potential welding defect that could cause bleeding or anastomotic leak.
Zimmer Biomet is recalling 19,483 M/DN Intramedullary Fixation Humeral Guide Wires because the sterile packaging seal may fail, potentially compromising sterility.
Fuel Injection Technology is recalling Summit Racing Max 500-EFI systems because fuel injector O-rings may leak, increasing fire risk.
Maharaja Food Importers is recalling ELA ADA (Jack Fruit) because the label lists ghee but fails to declare milk, a major allergen.
BioFire Diagnostics is recalling the FilmArray BCID Panel because it may produce false positive Proteus results when used with specific BD BACTEC blood culture bottles.
Synthes, Inc. is recalling 31 Stem Extractor f/Guide Bar units because the connection screw may break during use.