State
73,388 recalls have nationwide distribution and so reach Louisiana. 6,958 additional recalls listed Louisiana specifically in their distribution scope.
Of the 6,958 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 6,958 recalls whose distribution notice names Louisiana specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Kenover Marketing Corp. is recalling Mighty Sesame Organic Tahini over potential Salmonella contamination. Approximately 13,766 units were distributed to stores across 20 states.
Philips Respironics Amara View Full-Face Mask lacks critical safety warnings about magnetic components for patients with implantable medical devices. The Class I recall affects 5.6 million units worldwide.
Philips Respironics is recalling the Therapy Mask 3100 NC/SP because the product lacks warnings about magnetic components that may affect patients with implantable devices or metallic splinters in the eyes.
Philips Respironics is recalling Wisp and Wisp Youth nasal masks because they lack warnings about magnetic components that could interfere with implanted medical devices or cause eye injuries from metallic splinters.
Cipla recalls Arformoterol Tartrate Inhalation Solution due to environmental monitoring failure affecting sterility assurance.
Eden's Answers Inc is recalling Sprigs Lil Ones Sleepy Time herbal supplement due to high bacterial growth in the product. Consumers should stop using it immediately.
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Philips has recalled MR Patient Care Portal 5000 desktop units (Model 453564792561) due to intermittent audio failure. The device may fail to produce audio, and standard troubleshooting does not reliably resolve the issue.
Eden's Answers Inc is recalling Sprigs Dental Health, an herbal dietary supplement, due to detection of high bacterial growth. The product was distributed across 37 states.
Eden's Answers Inc is recalling Sprigs Honey Herbal Syrup dietary supplement due to high bacterial growth within the product. The affected product was distributed across multiple states.
Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.
AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.
FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.
Kia is recalling certain 2021-2023 K5 and 2021-2022 Sorento vehicles with transmission oil pump malfunction that may cause complete loss of drive power, increasing crash risk.
Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.
Chrysler is recalling specific Mopar brake hoses because the inside diameter may be too small, causing rupture and loss of braking ability.
Wabash National is recalling 2020-2023 RFALHSA trailers because the lift gate obscures rear conspicuity tape, reducing visibility and increasing crash risk.
Fontaine is recalling 56 Elgin sweepers because a braided air line may rub through an oil tube, causing pump failure and loss of power.