State
73,741 recalls have nationwide distribution and so reach Louisiana. 6,965 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,965 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 6,965 recalls whose distribution notice names Louisiana specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Angiotech is recalling 500 units of Double Diamond J Type Bone Marrow Needles due to a manufacturing defect in the sterile seal on blister trays.
Angiotech is recalling 180 units of J Type Bone Marrow Needles due to a manufacturing issue affecting the sterile seal on blister trays.
GE Healthcare is recalling Centricity Universal Viewer Breast Imaging software because a display error could lead to incorrect patient diagnoses.
Stryker is recalling Naera Hospital Bassinet mattresses because air expansion at high altitudes may create gaps, posing a risk of patients rolling over.
Bard Medical Division is recalling 450 units of SureStep Foley Tray Systems because the sample ports may leak urine.
Abbott Ireland Diagnostics Division is recalling ARCHITECT Free T3 Reagent Kits because reagent carryover may cause depressed test results on specific platforms.
US Pharmaceuticals is recalling Soothe & Cool Protect Moisture Guard Skin Protectant due to out-of-specification microbial counts in purified water.
Richard Wolf GmbH is recalling 873 Bronchoscope Tubes, Model Texas, because non-functional bonding points may loosen. The devices are used for respiratory tract investigation and therapy.
US Pharmaceuticals is recalling Medline Remedy Barrier Skin Protectant Ointment due to out-of-specification microbial counts in purified water.
Angiotech is recalling 1,260 bone marrow biopsy needles due to a manufacturing issue affecting the sterile seal on blister trays.
Angiotech is recalling 1,404 Bone Marrow Biopsy Needles due to a manufacturing defect in the sterile seal on blister trays.
US Pharmaceuticals is recalling Hydrocortisone Cream Intensive Healing due to out-of-specification microbial counts in purified water.
Abbott Ireland Diagnostics Division is recalling ARCHITECT Total T3 Reagent Kits because reagent carryover may cause depressed test results on specific platforms.
Angiotech is recalling 2,502 bone marrow biopsy needles due to a manufacturing issue affecting the sterile seal on blister trays.
Lupin Pharmaceuticals is recalling Bimatoprost Ophthalmic Solution 0.03% because out-of-specification results were observed for individual and total impurities.
Daimler Trucks North America is recalling 2013-2016 Freightliner Cascadia trucks because brake vibrations may cause tie-rod failure, leading to loss of steering.
Target is recalling Cat & Jack toddler boots because the unicorn horn can detach, posing a choking hazard to children.
Ford is recalling 2017-2019 Lincoln Continental vehicles because door latch motors may fail, preventing doors from fully engaging and increasing injury risk.
Forest River is recalling 2019 Columbus recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.
Ford is recalling 2011-2013 F-150 trucks with 6-speed automatic transmissions because they may unexpectedly downshift into first gear, increasing crash risk.
ASA Electronics is recalling Voyager monitors that may revert to factory settings, causing the backup camera image to reverse and increasing crash risk.
Blue Bird is recalling one 2019 Vision bus because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.
Lakota is recalling 2018-2019 Bighorn, Charger, Colt, and Livestock Edition trailers because incorrect tire data on the Federal Placard could lead to tire overload and failure.
Forest River is recalling 2019 Wildwood recreational trailers because the Federal Placard lists an incorrect front tire pressure of 110 PSI instead of 80 PSI.
Ford is recalling 2019 Mustang, Lincoln Nautilus, and Navigator vehicles because the instrument cluster may display blank, hiding critical safety information.