Louisiana recalls
3,504 federal recalls affecting Louisiana in the last 12 months - 150 Louisiana-specific plus 3,354 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-01FDA-FoodSpring & MulberryClass INationwideSpring & Mulberry Mint Leaf Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a teal green cardboard box, UPC 850055470217, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individually or as a 3-pk, 6-pk, or 12-pk (Amazon only).
Potential Salmonella contamination
- 2026-07-01FDA-FoodChampion FoodsClass IINationwideMotor City Pizza Co. 5 Cheese Bread recalled for Salmonella risk
Motor City Pizza Co. 5 Cheese Bread products may contain Salmonella, a bacteria that can cause serious illness. The affected products were distributed nationwide to major retailers including Costco, Walmart, Target, and Kroger.
- 2026-07-01FDA-FoodPrime Food ProcessingClass IPrime Food Processing dried herring recalled for botulism risk
Prime Food Processing dried herring fish (7 oz.) was not properly cleaned before drying, which can allow Clostridium botulinum bacteria to grow. This bacterium produces a toxin that causes botulism, a serious foodborne illness. The affected product has lot code 26020 with expiration date 06.12.28.
- 2026-07-01FDA-DrugSun PharmaceuticalClass IINationwideSun Pharmaceutical Perampanel recalled for tablet strength mix-up
Sun Pharmaceutical discovered that some bottles labeled as containing 6mg Perampanel tablets actually contained 10mg tablets instead. This mix-up affects one lot (AE01763) distributed nationwide. Patients taking the wrong strength could receive an incorrect dose of this seizure medication.
- 2026-07-01FDA-DrugElevate Oral CareClass IINationwideElevate Oral Care Povi-One recalled for sub-potency
Elevate Oral Care's Povi-One 10% Povidone-Iodine Oral Antiseptic does not contain the full strength stated on the label. Five specific production lots distributed nationwide do not meet the required potency standard, which means the product may not work as intended for oral antiseptic purposes.
- 2026-07-01FDA-DrugAnnora PharmaClass IINationwideCamber Lacosamide tablets recalled for Selexipag mix-up
Some bottles of Lacosamide 100mg tablets may contain Selexipag 1000 mcg tablets instead. This mix-up happened during manufacturing and could cause patients to take the wrong medication. The recall affects specific lots distributed nationwide.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep FREPP Clear recalled for sterility concerns
BD ChloraPrep FREPP Clear, a sterile skin antiseptic applicator, may contain fungal contamination (Aspergillus penicillioides) or may not be fully sterile due to wrinkles in the packaging seal. Approximately 178,000 applicators from lot 4073005 (expiring 03/31/2027) are affected nationwide and internationally.
- 2026-07-01FDA-DrugCareFusionClass INationwideBD ChloraPrep Clear recalled for fungal contamination risk
BD ChloraPrep Clear, a sterile antiseptic skin-prep solution used before medical procedures, was found to contain Aspergillus penicillioides fungus in some applicators. This affects the sterility of the product, which is critical for medical use. The affected lot is Lot #4032183 with an expiration date of January 31, 2027.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep FREPP Clear recalled for sterility risk
BD ChloraPrep FREPP Clear applicators may have wrinkles in the paper lid that could compromise the sterile seal. This affects multiple lot numbers distributed nationwide through mid-2027. No injuries have been reported.
- 2026-07-01FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for sterility assurance concern
BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, is being recalled because wrinkles in the paper packaging lid may allow the sterile seal to be breached. This defect could potentially allow contamination of the product. No injuries have been reported.
- 2026-07-01FDA-DrugANI PharmaceuticalsClass IIINationwideANI Pharmaceuticals hydroxyzine solution recalled for foreign substance
ANI Pharmaceuticals is recalling hydroxyzine hydrochloride oral solution (10 mg/5 mL, 473 mL bottles) due to the presence of a foreign substance in one lot. The affected product was distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugDirect RxClass IINationwideDirect Rx Duloxetine D/R recalled for impurity risk
Direct Rx's packaged Duloxetine D/R 30 mg capsules contain levels of N-nitroso-duloxetine, a potentially harmful impurity, above FDA's recommended limit. This is a manufacturing quality issue affecting specific lots distributed nationwide.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar cinacalcet tablets recalled for manufacturing deviations
Amgen is recalling Sensipar (cinacalcet) 90mg tablets due to deviations from current good manufacturing practice (CGMP) standards. This affects one lot distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Corlanor recalled for foreign substance contamination
Amgen is recalling specific lots of Corlanor (ivabradine) 7.5mg tablets due to the presence of a foreign substance in some bottles. The affected lots were distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar tablets recalled for manufacturing deviations
Amgen is recalling Sensipar (cinacalcet) 60mg tablets due to deviations from manufacturing standards. The recall affects one lot (1157055) with an expiration date of January 31, 2028, distributed nationwide.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Sensipar recalled for manufacturing quality deviations
Amgen is recalling Sensipar (cinacalcet) 30mg tablets due to deviations from manufacturing quality standards (CGMP). The recall affects one specific lot distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAmgenClass IINationwideAmgen Corlanor heart medication recalled for foreign substance
Amgen has recalled multiple lots of Corlanor (ivabradine) 5 mg tablets due to the presence of a foreign substance in some bottles. The affected tablets are packaged in 14-tablet and 60-tablet bottles distributed nationwide. No injuries have been reported.
- 2026-07-01FDA-DrugAjanta PharmaClass IINationwideAjanta Pharma fenofibrate capsules recalled for quality issues
Ajanta Pharma USA Inc. is recalling one lot of fenofibrate 200 mg capsules due to manufacturing quality deviations discovered during inspection. The affected lot (PA02216, expiring 12/2029) was distributed nationwide.
- 2026-07-01FDA-DrugThe Harvard DrugClass IINationwideMajor Pharmaceuticals Methylergonovine Maleate recalled for subpotency
MAJOR Pharmaceuticals is recalling Methylergonovine Maleate Tablets, USP, 0.2 mg due to subpotency — meaning the tablets contain less active ingredient than labeled. The affected lots were distributed nationwide. This is a prescription medication used to control bleeding after childbirth.
- 2026-06-25FDA-PRRevival Animal HealthNationwideBreeder's Edge and Shelter's Choice dog milk replacers recalled for vitamin D risk
Revival Animal Health is recalling several canine and goat milk replacer products because they contain inconsistent levels of vitamin D—some too low, some too high. Dogs fed these products may develop serious health problems ranging from vomiting and weakness to bone deformities (rickets in puppies) or kidney damage (from excess vitamin D). Two cases of rickets have been reported so far.
- 2026-06-25FDA-PRLehi Valley TradingNationwideHigh Valley Orchard raisins recalled for undeclared peanuts
Lehi Valley Trading Company recalled 624 units of High Valley Orchard Chocolate Covered Raisins (15 ounce packages) because they contain undeclared peanuts. The affected product has lot #0160933 and a best-by date of January 23, 2027. A temporary breakdown in production and packaging processes caused the contamination.
- 2026-06-25CPSCTreatlifeNationwideTreatlife smoke and CO detectors recalled for fire alert failure
Treatlife smoke and carbon monoxide detectors can fail to sound an alarm when smoke or fire is detected. These white, circular detectors are powered by AA batteries and were sold on Amazon. The failure to alert poses a risk of serious injury or death from smoke inhalation or burns.
- 2026-06-25CPSCDaikinNationwideAmana air conditioners and heat pumps recalled for fire risk
Certain Amana brand window and through-the-wall air conditioners and heat pumps can experience a ground fault that leaves the heating element energized even after the unit is turned off. This poses a risk of fire or burn injury. One report of plastic melting on a unit has been received, though no injuries have occurred so far.
- 2026-06-25CPSCABGA Advanced TradingNationwideHonlyne LED party favors recalled for battery ingestion risk
Honlyne LED party favors sold on Amazon contain button cell batteries in compartments that children can easily access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.
- 2026-06-25CPSCSmall FishNationwideSmall Fish Busy Board recalled for magnet ingestion risk
Small Fish Montessori Busy Board toys (model 2512JX02) contain magnets that can detach and be swallowed by children. When multiple magnets are ingested, they can attract each other inside the digestive system, causing serious injury or death from intestinal perforation, blockage, or infection.
- 2026-06-25CPSCCarinaNationwideRaychy light-up children's sneakers recalled for battery ingestion risk
These light-up sneakers contain coin batteries that children can easily access and swallow. Ingesting these batteries can cause serious internal burns and other life-threatening injuries. The sneakers lack required safety warnings and do not meet federal battery safety standards.
- 2026-06-25CPSCShield LineNationwideMedPride Baby Oil recalled for child poisoning risk
MedPride Baby Oil bottles do not have child-resistant caps as required by law. Young children can open the bottle and swallow the oil, which contains petroleum distillates that can cause serious poisoning, chemical pneumonia, and potentially fatal lung damage.
- 2026-06-25CPSCVeseackyNationwideVeseacky Lomi waxing kits recalled for burn and fire hazard
The Lomi Roll-On Waxing Kit (models LOMB2003PK and LOMB2004PK) does not meet safety standards for flammability and presents a risk of burns or fire. These handheld wax warmers were sold online through Amazon from October 2020 through January 2026. About 14,700 units are affected.
- 2026-06-25CPSCSpectorNationwideSpector & Co. solar power banks recalled for overheating risk
The lithium-ion battery in the Super Off-Road 12,000 mAh Solar Wireless Power Bank can swell and overheat, creating a burn hazard. The company has received two reports of battery swelling. About 7,400 units were distributed as promotional items between January 2019 and December 2023.
- 2026-06-25CPSCYongkang RuiheNationwideYamazuki Sunderwell youth ATVs recalled for missing brake lights
Yamazuki's Sunderwell brand youth ATVs (model XW-A17) sold online lack brake lights, making them harder for other vehicles to see. This visibility gap increases the risk of crashes and serious injury. About 200 units were sold between October and December 2025.
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