State
73,596 recalls have nationwide distribution and so reach Louisiana. 6,960 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,960 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 6,960 recalls whose distribution notice names Louisiana specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Little Loves & Co. is recalling youth clothing sets with drawstrings due to an entrapment hazard that could cause serious injury or death to children.
Whole Foods Market is recalling Spicy Guacamole Dip No Tomatoes because the jalapeños used may be contaminated with Salmonella. The product was sold in 13 states.
Whole Foods Trio Dip is being recalled because the jalapeños used in the product may be contaminated with Salmonella.
Whole Foods Market is recalling Mild Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Whole Foods Market is recalling Roasted Corn Guacamole Dip because it was made with jalapenos that may be contaminated with Salmonella.
Whole Foods Market is recalling Medium Pico de Gallo Guacamole Dip because it may contain jalapenos contaminated with Salmonella.
Fresenius Kabi is recalling 625,500 Morphine Sulfate syringes because some were mislabeled and contained Dilaudid instead.
Whole Foods Market is recalling Spicy Guacamole Dip because the jalapenos used may be contaminated with Salmonella.
Coast Citrus Distributors is recalling bulk jalapeno peppers due to potential Salmonella Javiana contamination. The product was distributed to wholesale distributors and has not been sold at retail.
Whole Foods Market is recalling Mild Guacamole Dip No Tomatoes because it may contain jalapenos contaminated with Salmonella.
Whole Foods Market is recalling Pomegranate Guacamole Dip because it may contain jalapenos contaminated with Salmonella. The product was sold in 13 states.
American Regent, Inc. is recalling Papaverine Hydrochloride Injection due to the presence of glass and/or paraformaldehyde particulate matter.
Whole Foods Market is recalling Mango Pineapple Salsa used in Caribbean Turkey Burgers because the jalapenos may be contaminated with Salmonella.
Dairyland Produce, LLC is recalling specific lots of jalapenos due to potential Salmonella contamination. Consumers in Louisiana and Texas should check their bags for the listed lot codes.
Whole Foods Market is recalling Heirloom Tomato Salsa because it was made with jalapenos that may be contaminated with Salmonella.
Boston Scientific is recalling ENROUTE Transcarotid Neuroprotection System Plus catheters due to a potential for arterial sheath tip separation during use.
American Regent is recalling Multrys (Trace Elements Injection 4) vials due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling 43,460 vials of Nicardipine Hydrochloride Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Cyanocobalamin injections due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling specific lots of Acetylcysteine Solution, USP, 10% due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
American Regent, Inc. is recalling Selenious Acid Injection due to the presence of particulate matter, including hair, glass, and paraformaldehyde.
Tobii Dynavox is recalling TD Navio Maxi Speech Generating Devices because damaged battery tabs may cause internal short circuits, heating, and gas venting.
American Regent, Inc. is recalling Cyanocobalamin injections because they contain particulate matter, including hair, glass, and paraformaldehyde.
Shilpa Medicare is recalling 18,434 vials of PEMRYDI RTU (pemetrexed injection) due to reports of green to dark green discoloration in the solution.
Bard Access Systems is recalling BD Needle Kits for Powered Drivers because the obturator may lock to the hub, potentially delaying emergency therapy.