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.
Siemens Healthcare Diagnostics is recalling specific IMMULITE assays because biotin interference is not documented in the instructions, potentially affecting test accuracy.
Siemens Healthcare Diagnostics is recalling IMMULITE Gastrin assays because biotin interference is not listed in the instructions for use.
Kroger Specialty Pharmacy is recalling Temozolomide 250 mg capsules due to a lack of processing controls. The recall affects specific lots dispensed between December 2017 and February 2018.
Kroger Specialty Pharmacy is recalling Dupixent 300 mg/2 mL prefilled syringes due to a lack of processing controls. The recall affects units dispensed in five states between December 2017 and February 2018.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur HBc IgM tests because the instructions do not list the biotin concentration limit, making the assay susceptible to interference.
Kroger Specialty Pharmacy is recalling Prolia 60 mg/1 mL syringes due to a lack of processing controls. The affected units were dispensed in five states.
Straumann Manufacturing is recalling Emdogain multipacks because a raw material shelf-life change was implemented without submitting data to demonstrate continued product efficacy.
Kroger Specialty Pharmacy is recalling MVW Complete Softgels and Chew Vitamins due to a lack of processing controls.
Kroger Specialty Pharmacy is recalling Vosevi 400/100/100 mg tablets due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.
Bard Peripheral Vascular Inc is recalling 10 units of POWERPORT ClearVUE Slim Implantable Port kits because the included Patient ID Card contains incorrect port flushing instructions.
Siemens Healthcare Diagnostics is recalling specific IMMULITE assays because biotin can interfere with results, potentially affecting patient care.
Kroger Specialty Pharmacy is recalling Dexamethasone 4 mg tablets due to a lack of processing controls. The affected products were dispensed in five states.
Siemens Healthcare Diagnostics is recalling IMMULITE Gastrin assays because biotin interference is not listed in the instructions for use.
Kroger Specialty Pharmacy is recalling Kitabis Pak 300 mg/5 mL Soln due to a lack of processing controls. The product was distributed in five states.
Mako Surgical Corporation is recalling 126 Restoris MCK Tibial Baseplates due to incorrect sizing labels. The devices were distributed to facilities in the US and several international countries.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 BR-MA (CA15-3) assays because biotin interference is not listed in the instructions for use.
Kroger Specialty Pharmacy is recalling Revlimid 10 mg oral capsules due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.
Randox Laboratories is recalling Lipase Assay kits due to potential contamination risks on Rx instruments. The recall affects specific lots distributed in West Virginia and Puerto Rico.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal systems because the adhesive may not meet specifications, causing patches to stick poorly to the skin.
American Custom Golf Cars is recalling 2016-2017 ACG Moke low speed vehicles because missing rear side red reflectors reduce visibility to other drivers.
PerkinElmer is recalling NeoBase Succinylacetone Assay Solution because leaking vials may cause minor allergic skin reactions if proper attire is not used.
Kroger Specialty Pharmacy is recalling Orkambi 200 mg/125 mg tablets dispensed in five states due to a lack of processing controls.
Kroger Specialty Pharmacy is recalling Repatha 140 mg/mL Sureclick AI 2-pk due to lack of processing controls. The recall affects units dispensed in MS, LA, AR, IL, and FL.
Bard Peripheral Vascular Inc is recalling 359 units of POWERPORT ClearVUE implantable ports because the included patient ID card contains incorrect flushing instructions.
Kroger Specialty Pharmacy is recalling Orkambi 100 mg/125 mg tablets due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.