State
73,509 recalls have nationwide distribution and so reach Louisiana. 6,959 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,959 recalls naming Louisiana we have scored against our rubric, 1,109 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,737 (25%) are Severe.
Which agencies issued them
These figures cover only the 6,959 recalls whose distribution notice names Louisiana specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Olympus Corporation is recalling 431 BF-Q180-AC EVIS EXERA II Bronchovideoscopes to issue validated reprocessing instructions aligned with FDA 2015 guidance.
Washington Homeopathic Products is recalling Haloderm Homeopathic Blend due to out-of-specification test results from identification testing. The product was distributed nationwide.
The uMI 550 medical imaging system may occasionally freeze during the EXAM acquisition workflow when a PET scan is canceled. This can disrupt clinical operations.
The uEXPLORER PET/CT System is being recalled because the EXAM acquisition workflow may freeze after canceling a PET scan. Affected systems may experience workflow interruptions during diagnostic imaging.
Washington Homeopathic Products is recalling Quebracho homeopathic pills in multiple potencies because testing identified out-of-specification results during identification analysis.
Washington Homeopathic Products is recalling Strophanthus hisp 30X Hives pills after testing identified out-of-specification results in identification tests. The recall affects approximately 91 bottles distributed nationwide.
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 60+) due to current good manufacturing practice (cGMP) deviations. The recall is voluntary and affects nationwide distribution in the US.
Washington Homeopathic Products is recalling ZTE 1015 Formula due to out-of-specification test results from identification testing. The product failed HPTLC analysis.
Washington Homeopathic Products is recalling Humulus 6X and 15X homeopathic pills distributed nationwide due to out-of-specification test results from identification testing.
Washington Homeopathic Products is recalling Aconitum napellus Fear pills in multiple potencies nationwide due to failed identification testing by high-performance thin-layer chromatography (HPTLC).
Olympus is updating reprocessing instructions for the BF-N20 Bronchofiberscope to comply with FDA 2015 guidance on medical device reprocessing validation.
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Invisible Daily Defense body spray sunscreen (SPF 60+) due to cGMP deviations. The recall affects approximately 88,380 cans distributed nationwide.
Johnson & Johnson Consumer is voluntarily recalling Neutrogena Ultra Sheer body mist sunscreen SPF 100+ nationwide due to manufacturing deviations. Approximately 3.98 million cans are affected.
Johnson & Johnson Consumer, Inc. is voluntarily recalling Neutrogena Ultra Sheer body mist sunscreen SPF 30 due to current good manufacturing practice (cGMP) deviations. The recall affects approximately 1.6 million cans distributed nationwide.
Washington Homeopathic Products is recalling ZTE-1035 Formula, an antimicrobial homeopathic combination product, due to out-of-specification test results for identification testing based on HPTLC analysis.
Johnson & Johnson Consumer, Inc. is recalling Neutrogena Beach Defense water+sun protection sunscreen spray (SPF 70) nationwide due to cGMP deviations. This is a voluntary recall initiated by the manufacturer.
Washington Homeopathic Products is recalling Althaea Officinalis 6X Irritable Bladder Sucrose/Lactose Pills distributed nationwide because test results failed to confirm the product's identity using HPTLC analysis.
Johnson & Johnson Consumer, Inc. is recalling 678,384 cans of Neutrogena COOLDRY SPORT sunscreen spray nationwide due to current Good Manufacturing Practice (cGMP) deviations.
Johnson & Johnson Consumer, Inc. is recalling Neutrogena COOLDRY SPORT WITH MICROMESH SUNSCREEN SPRAY (5.5 oz, SPF 50) due to cGMP (current Good Manufacturing Practice) deviations. Approximately 1.4 million cans distributed nationwide are affected.
Hobby Lobby is recalling about 14,000 White Wood Stools sold nationwide from June through July 2021 because the stools can break during use, posing fall and injury hazards. Hobby Lobby has received seven reports of the stool breaking, including six resulting in minor injuries.
Johnson & Johnson is recalling Neutrogena COOLDRY SPORT sunscreen spray SPF 30 in two sizes nationwide due to cGMP (current Good Manufacturing Practice) deviations. The recall affects approximately 469,764 cans.
Johnson & Johnson Consumer is recalling Neutrogena Beach Defense water + sun protection sunscreen spray in two sizes (6.5 oz and 8.5 oz) nationwide due to current good manufacturing practice (cGMP) deviations.
American Health Packaging is recalling Valproic Acid Oral Solution due to potential microbial contamination in liquid sugar batches used during manufacturing. The affected product was distributed nationwide.
Washington Homeopathic Products is recalling Viola Odorata homeopathic medicine (Lot #29057, expiration 8/17/2026) distributed nationwide because identification testing using HPTLC analysis returned out-of-specification results.
Olympus Corporation has issued new, validated reprocessing instructions for the BF-P60 OES Bronchofiberscope to comply with FDA guidance. The recall affects 1,030 devices distributed nationwide and internationally.