State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
BMW is recalling 2020 X5 and X7 vehicles because steering rack pinion teeth may break, causing loss of steering control and increasing crash risk.
Arcos, Inc. is recalling 28 Burn Navigator H2 units because their battery packs may heat up abnormally and ignite in rare instances.
Pierce Manufacturing is recalling one 2019 Pierce Tanker vehicle because insufficient front axle lubrication may damage wheel end bearings, potentially causing wheel separation and loss of control.
ZF North America is recalling aftermarket steering center rods for 1996-2004 BMW 5 Series vehicles due to a risk of detachment causing loss of steering control.
Green Water, LLC is recalling specific lots of Taspen's Organics herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Siemens Healthcare Diagnostics is recalling N Cuvette Segments for the BN ProSpec System because they may produce falsely elevated albumin results.
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Green Water, LLC is recalling Taspens Organics tea and herbal tinctures due to potential Salmonella contamination. The products were distributed nationwide.
Thoratec Corp. is recalling 149 Heartmate 3 Sealed Outflow Graft units because the C-Ring may not seat properly, causing leaks during implantation.
TiSport is recalling 1,452 TiLite wheelchairs because the anti-tip tubes may fail, allowing the chair to tip backwards.
Siemens is recalling IMMULITE 2000 Progesterone tests because some samples may produce falsely low results, potentially leading to unnecessary medication.
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Green Water, LLC is recalling several herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Siemens is recalling 44 MAGNETOM Skyra MRI devices due to a potential open port in the quench venting system when using an optional horizontal outlet.
Qiagen is recalling QIAsymphony SP software version 5.0.3 because it incorrectly assigns 2D barcode eluate IDs to samples, which could lead to incorrect patient reporting.
Siemens is recalling IMMULITE 1000 Progesterone tests because they may produce falsely low results, potentially leading to unnecessary progesterone supplementation.
DeRoyal Industries is recalling specific polyurethane feeding tubes because the connector may detach from the tube.
Green Water, LLC is recalling specific lots of herbal tinctures and teas due to potential Salmonella contamination. The products were distributed nationwide.
Luminex is recalling Aries M1 barcode scanners due to incorrect control boards that could cause patient sample mismatches or duplicate results.
Becton Dickinson is recalling BD Vacutainer Lithium Heparin blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with specific instruments.
Becton Dickinson is recalling BD Vacutainer LH blood collection tubes because they can cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Becton Dickinson is recalling specific blood collection tubes because they may cause false elevation of carboxyhemoglobin results when used with the IL GEM 4000 instrument.
Becton Dickinson is recalling specific blood collection tubes because they may cause falsely elevated carboxyhemoglobin results when used with the IL GEM 4000 instrument.