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 ADVIA Centaur Folate assays because biotin interference levels are not listed in the instructions, potentially affecting test accuracy.
Siemens Medical Solutions is recalling Syngo.Via VB20A software because corrected report values are not saved or transmitted, causing the system to use original values.
Bard Peripheral Vascular Inc is recalling 3,196 units of POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Bard Peripheral Vascular Inc is recalling POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Kroger Specialty Pharmacy is recalling Kisqali 200 mg tablets dispensed in five states due to a lack of processing controls.
Grato Holdings, Inc. is recalling Energique Enervimin CNCR Focus dietary supplements because they are unapproved new drugs based on disease claims.
Kroger Specialty Pharmacy is recalling Kalydeco 150 mg tablets dispensed in five states due to a lack of processing controls.
Kroger Specialty Pharmacy is recalling OPDIVO 40 mg/4 mL SDV due to a lack of processing controls. The affected product was dispensed in five states between December 2017 and February 2018.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Folic Acid assays because biotin interference is not listed in the instructions for use.
Siemens Healthcare Diagnostics is recalling IMMULITE CEA assays because biotin interference thresholds are not listed in the instructions, potentially affecting test accuracy.
Kroger Specialty Pharmacy is recalling Revlimid 15 mg oral capsules due to a lack of processing controls. The affected units were dispensed in five states between December 2017 and February 2018.
Straumann Manufacturing is recalling Emdogain Enamel Matrix Derivative because a raw material shelf life change was implemented without submitting data to demonstrate continued product efficacy.
Kroger Specialty Pharmacy is recalling Xalkori 250 mg capsules due to a lack of processing controls. The affected lots were dispensed in five states between December 2017 and February 2018.
Kroger Specialty Pharmacy is recalling Promacta 50 mg tablets due to a lack of processing controls. The recall affects specific lots dispensed in five states.
MHC Medical Products LLC is recalling EasyTouch Insulin Syringes because retail cartons may display incorrect lot numbers.
Beckman Coulter is recalling 2,225 iChemVELOCITY Urine Chemistry Systems because incorrect settings may cause false low results or incorrect color reporting.
Bard Peripheral Vascular Inc is recalling 4,044 POWERPORT ClearVUE catheters because the Patient ID Card contains incorrect port flushing instructions.
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Allergy specific IgE Universal Kits because biotin interference is not documented in the instructions for use.
Kroger Specialty Pharmacy is recalling Stelara 90 mg/MI PFS due to lack of processing controls. The recall affects units dispensed in five states between December 2017 and February 2018.
Kroger Specialty Pharmacy is recalling Ibrance 125 mg capsules due to a lack of processing controls. The recall covers units dispensed in five states between December 2017 and February 2018.
Bard Peripheral Vascular Inc is recalling 216 units of POWERPORT ClearVUE Slim catheters because the packaged Patient ID Card contains incorrect port flushing instructions.
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive may not stick well to the skin.
Kroger Specialty Pharmacy is recalling Altera Handset due to a lack of processing controls. The product was distributed in five states.
Kroger Specialty Pharmacy is recalling Sodium Chloride 3% Inhalation Solution due to a lack of processing controls. The product was distributed in five states.
Siemens Healthcare Diagnostics is recalling IMMULITE Vitamin B12 assays because biotin interference is not listed in the instructions for use.