Louisiana recalls
4353 federal recalls on file affecting Louisiana - 436 Louisiana-specific plus 3917 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Introducer Kit recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP introducer recalled for leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella RP Flex recalled for sheath leakage risk
A potential for introducer sheath leakage from under the sheath cap and along the hub score lines, identified in 14Fr and 23Fr Introducers. These manufacturing issues are not visually detectable by the user, and 14Fr or 23Fr Introducers are provided in every pump set.
- 2026-07-22FDA-FoodGeneral MillsClass IIPillsbury Kaiser Roll Dough recalled for glass risk
Potential foreign material (glass)
- 2026-07-22FDA-FoodGeneral MillsClass IIPillsbury Hard Roll Dough recalled for glass risk
Potential foreign material (glass)
- 2026-07-22FDA-FoodNutriciaClass IINutricia NOURISH meal replacement formula recalled for low vitamin A
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- 2026-07-22FDA-FoodNutriciaClass IINutricia Liquid Hope formula recalled for low Vitamin A
Subpotent for Vitamin A. The firm discovered that the testing laboratory used the wrong method when testing for Vitamin A. The test results gave a higher concentration of vitamin A than what is actually in the product.
- 2026-07-22FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for packaging seal defect
Lack of Assurance of Sterility: Affected product may exhibit an open or incomplete seal on the packaging of the applicator
- 2026-07-22FDA-DrugChiesiClass IINationwideChiesi CLEVIPREX injection recalled for sterility concerns
Lack of Assurance of Sterility
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCAREone Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideMeijer Carbamide Peroxide oral rinse recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFoster & Thrive Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideLeader Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideGood Neighbor Pharmacy Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFAMILY Wellness Carbamide Peroxide recalled for subpotent formulation
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideAudiologist's Choice Carbamide Peroxide recalled for low potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideTopCare Health Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideQC Quality Choice Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideClinere Carbamide Peroxide recalled for reduced strength
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCVS Health Carbamide Peroxide recalled for reduced potency
SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).
- 2026-07-22FDA-DrugPadagisClass IINationwidePadagis Nystatin Cream recalled for reduced potency
Subpotent Drug: Low out of specification assay results performed during long-term stability testing.
- 2026-07-21FDA-PRPT OrganicsNationwidePumpkin Tree Peter Rabbit Organics recalled for soft plastic risk
July 21st, 2026, PT Organics Limited of Lake Oswego, Oregon is voluntarily recalling select Pumpkin Tree Peter Rabbit Organics Banana & Strawberry 4 oz. (113 g) pouches because of an internal packaging defect that may result in the presence of a strand of soft, food-grade plastic in the finished pro
- 2026-07-19FDA-PRRelay Peak Research LLCNationwideZen Principle Moringa Capsules recalled for Salmonella risk
Relay Peak Research LLC (Zen Principle Naturals) of Incline Village, NV is voluntarily recalling its Zen Principle® brand Moringa Capsules dietary supplement because the product has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections i
- 2026-07-18FDA-PRUnique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)NationwideUnique Pharmaceutical cetirizine tablets recalled for ranitidine contamination
FOR IMMEDIATE RELEASE – July 18th, 2026 – Panoli, Gujarat, Unique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.) is voluntarily recalling four lots of Cetirizine Hydrochloride Tablets USP 5 mg to the consumer level due to cross contamination with Ranitidine.
- 2026-07-17FDA-PRTaylor Fresh FoodsTaylor Fresh Foods iceberg lettuce recalled for Cyclospora risk
Taylor Farms de Mexico of Guanajuato, Mexico is voluntarily removing all iceberg lettuce sourced from central Mexico from the U.S. market, because it has the potential to be contaminated with Cyclospora. Most people infected with Cyclospora develop diarrhea, with frequent bowel movements. Other comm
- 2026-07-16CPSCZhuzhoushizuisuanshangmaoyouxiangongsi, of ChinaNationwideMNIENT portable bed rails recalled for entrapment risk
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. The bed rails do not meet structural stability or retention strap requirements, posing a fall hazard. Additionally, the bed rails' push pins and push pin holes are incorrectly sized, posing a laceration hazard.
- 2026-07-16CPSCTargetNationwideTarget Cat & Jack sandals recalled for choking hazard
The sandals' decorative pearls can fall off, posing a risk of serious injury or death from a choking hazard.
- 2026-07-16CPSCYiwushi Bihe Trading Co., Ltd., of ChinaNationwideSDADI kitchen step stools recalled for entrapment and collapse risk
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and death due to tip over, fall and entrapment hazards.
- 2026-07-16CPSCDongguan Shinneng Huizheng Network Technology Co., Ltd., dba HurzeinNationwideNoerishia bed rails recalled for entrapment and asphyxiation risk
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
- 2026-07-16CPSCMadewell Inc., of Wenzhou Zhongbang Smoking Set Manufacturing Co., Ltd., doing business as Jobon Official Store, of ChinaNationwideJobon torch lighters recalled for burn and fire hazard
The lighters violate the mandatory safety standard for multipurpose lighters because they do not have the required child-resistant mechanisms posing a risk of serious injury or death from fire and burn hazards. In addition, the lighters failed to meet the pre-market lighter submission requirement needed to demonstrate that the lighters feature child-resistant mechanisms and ensuring their safety and compliance with U.S. regulations.
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