Alaska recalls
3,404 federal recalls affecting Alaska in the last 12 months - 56 Alaska-specific plus 3,348 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for sheath leakage risk
Abiomed has recalled certain Impella 5.5 SmartAssist S2 heart pump sets worldwide due to a manufacturing defect in the introducer sheaths. The 14Fr and 23Fr introducers included in these pump sets may leak fluid from under the sheath cap or along hub seams, and the leakage cannot be seen by the user before or during use.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella 5.5 heart pump recalled for leakage risk
The Abiomed Impella 5.5 Smart Assist Set heart pump contains an introducer sheath that may leak under the cap or along hub seams. This manufacturing defect is not visible to the user but is present in all affected pump sets. The issue affects 383 units distributed worldwide.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Introducer Kit recalled for sheath leakage risk
Abiomed has recalled certain Introducer Kit 23 Fr units (Pump Set Code 1000441) due to a potential for sheath leakage from under the sheath cap and along hub score lines. This manufacturing issue cannot be seen by the user and affects introducers included in every pump set.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP Introducer Kit recalled for leakage risk
Abiomed has recalled the Impella CP Introducer Kit (Pump Set Code 1000550) worldwide due to a potential for fluid leakage from under the sheath cap and along hub score lines in the 14Fr and 23Fr introducers. The leakage defect is not visible to the user and affects all current batches of this heart pump accessory kit.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella CP introducer recalled for leakage risk
Abiomed has recalled the Impella CP heart pump introducer due to a manufacturing defect that can cause fluid leakage from under the sheath cap and along the hub. The defect is not visible to the user and affects all current batches worldwide.
- 2026-07-22FDA-DeviceAbiomedClass INationwideAbiomed Impella RP Flex recalled for sheath leakage risk
The Abiomed Impella RP Flex heart pump set includes introducers that may leak fluid from under the sheath cap or along hub score lines due to manufacturing defects. These leaks cannot be seen by visual inspection. All current batches worldwide are affected.
- 2026-07-22FDA-FoodNutriciaClass IINutricia NOURISH meal replacement formula recalled for low vitamin A
Nutricia North America discovered that its testing laboratory used an incorrect method to measure vitamin A content in NOURISH ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY. The test results showed higher vitamin A levels than what is actually in the product, meaning affected packages contain less vitamin A than the label states.
- 2026-07-22FDA-FoodNutriciaClass IINutricia Liquid Hope formula recalled for low Vitamin A
Nutricia North America discovered that its testing lab used an incorrect method to measure Vitamin A in Liquid Hope Organic Whole Foods Meal Replacement Peptide Formula (Berry Medley). As a result, the product contains less Vitamin A than the label states. The affected pouches have best-if-used-by dates through March 15, 2028 (24-count cases) and October 7, 2027 (12-count packages).
- 2026-07-22FDA-DrugCareFusionClass IINationwideBD ChloraPrep Clear recalled for packaging seal defect
BD ChloraPrep Clear, a sterile skin antiseptic solution used before medical procedures, may have open or incomplete seals on individual applicator packaging. This could allow contamination of the sterile product. The issue affects multiple lot numbers distributed nationwide.
- 2026-07-22FDA-DrugChiesiClass IINationwideChiesi CLEVIPREX injection recalled for sterility concerns
Chiesi USA is recalling specific lots of CLEVIPREX (clevidipine) injectable emulsion because the manufacturer cannot guarantee the vials are sterile. This affects vials distributed nationwide with lot numbers 1239521 and 1237454, expiring in October 2027. No injuries have been reported.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCAREone Carbamide Peroxide recalled for reduced potency
CAREone Carbamide Peroxide 6.5% oral rinse (lot 1505141, expiring April 2027) contains significantly less active ingredient than labeled (~0.6% instead of ~6.5%) and has a lower pH than specified. The product may not work as intended for its intended use.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideMeijer Carbamide Peroxide oral rinse recalled for reduced potency
Meijer's Carbamide Peroxide 6.5% oral rinse (0.5 FL OZ, lot 1505344, expiration April 2027) contains significantly less active ingredient than labeled — approximately 0.6% instead of the expected 6–7%. The product also has a lower pH than specified. This means the rinse will not work as intended for oral care.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFoster & Thrive Carbamide Peroxide recalled for reduced potency
Foster & Thrive Carbamide Peroxide 6.5% oral rinse was found to contain significantly less active ingredient than labeled (~0.6% instead of ~6-7%), along with abnormally low pH. The affected product may not work as intended for its intended use. No injuries have been reported.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideLeader Carbamide Peroxide recalled for reduced potency
Some bottles and kits of Leader Carbamide Peroxide 6.5% contain significantly less active ingredient than labeled (about 0.6% instead of 6–7%) and have an abnormally low pH. The product may not work as intended for ear wax removal or oral rinse.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideGood Neighbor Pharmacy Carbamide Peroxide recalled for reduced potency
Good Neighbor Pharmacy Carbamide Peroxide 6.5% ear-cleaning solution was distributed with significantly reduced active ingredient (~0.6% instead of ~6–7%) and abnormal pH. The product may not work as intended for ear wax removal.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideFAMILY Wellness Carbamide Peroxide recalled for subpotent formulation
Bell Pharmaceuticals' FAMILY Wellness Carbamide Peroxide 6.5% oral rinse has been found to contain significantly less active ingredient than labeled (~0.6% instead of ~6–7%), and has a lower pH than specified. The affected lots will not work as intended for oral care.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideAudiologist's Choice Carbamide Peroxide recalled for low potency
Bell Pharmaceuticals distributed Audiologist's Choice Carbamide Peroxide ear cleaning solution with significantly reduced active ingredient—about 0.6% instead of the expected 6–7%—and abnormally low pH. This makes the product ineffective for its intended use.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideTopCare Health Carbamide Peroxide recalled for reduced potency
TopCare Health Carbamide Peroxide 6.5% oral rinse has significantly lower active ingredient than labeled (about 0.6% instead of 6–7%) and abnormal pH. The product may not work as intended for whitening or cleaning teeth.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideQC Quality Choice Carbamide Peroxide recalled for reduced potency
QC Quality Choice Carbamide Peroxide 6.5% oral rinse has significantly lower active ingredient levels than labeled (about 0.6% instead of 6–7%) and an unusually low pH. This means the product may not work as intended for oral care. The recall affects specific lots distributed nationwide.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideClinere Carbamide Peroxide recalled for reduced strength
Bell Pharmaceuticals is recalling Clinere Carbamide Peroxide ear cleaning solution due to manufacturing defects that reduced the active ingredient strength to approximately 0.6% instead of the expected 6–7%. The affected bottles also have a lower-than-normal pH. These defects may reduce the product's effectiveness.
- 2026-07-22FDA-DrugBell PharmaceuticalsClass IINationwideCVS Health Carbamide Peroxide recalled for reduced potency
CVS Health Carbamide Peroxide 6.5% oral rinse contains significantly less active ingredient than labeled (about 0.6% instead of 6–7%) and has an abnormally low pH. The product may not work as intended for oral care.
- 2026-07-22FDA-DrugPadagisClass IINationwidePadagis Nystatin Cream recalled for reduced potency
Padagis Nystatin Cream USP (100,000 units, 15 g tube, lot #205060, expiring 09/30/2027) has been recalled because stability testing found the active ingredient fell below the required strength specification. The cream may not work as effectively as intended to treat fungal infections.
- 2026-07-21FDA-PRPT OrganicsNationwidePumpkin Tree Peter Rabbit Organics recalled for soft plastic risk
PT Organics Limited is recalling select 4 oz. Pumpkin Tree Peter Rabbit Organics Banana & Strawberry fruit puree pouches sold at Kroger, Meijer, and Target between March and July 2026. An internal packaging defect may have allowed a strand of soft, food-grade plastic to enter some pouches. No injuries have been reported.
- 2026-07-19FDA-PRRelay Peak Research LLCNationwideZen Principle Moringa Capsules recalled for Salmonella risk
Zen Principle Moringa Capsules dietary supplement may be contaminated with Salmonella due to contamination in the moringa leaf powder ingredient. The affected product is Lot A6FF4 with a Best By date of 11/2028, distributed nationwide from December 2025 through July 2026 primarily online. No illnesses have been reported.
- 2026-07-18FDA-PRUnique Pharmaceutical Laboratories (A Div. of J. B. Chemicals & Pharmaceuticals Ltd.)NationwideUnique Pharmaceutical cetirizine tablets recalled for ranitidine contamination
Four lots of Unique Pharmaceutical Cetirizine Hydrochloride 5 mg tablets were found to be cross-contaminated with ranitidine. The contamination was discovered when pharmacy staff noticed red discoloration on some tablets. People with sensitivity to ranitidine could experience serious allergic reactions.
- 2026-07-16CPSCZhuzhoushizuisuanshangmaoyouxiangongsi, of ChinaNationwideMNIENT portable bed rails recalled for entrapment risk
MNIENT brand adult portable bed rails (model LQX-110055) do not meet safety standards and can trap users between the rail and mattress, posing a serious risk of injury or death by asphyxiation. The rails also have stability problems and incorrectly sized pins that can cause cuts.
- 2026-07-16CPSCTargetNationwideTarget Cat & Jack sandals recalled for choking hazard
Decorative pearls on Target's Cat & Jack children's sandals can fall off and pose a choking risk to young children. The tan sandals with raffia straps and gold buckles were sold in sizes 5T through 12T from January through May 2026. Target has received 23 reports of pearls falling off, though no injuries have been reported yet.
- 2026-07-16CPSCYiwushi Bihe Trading Co., Ltd., of ChinaNationwideSDADI kitchen step stools recalled for entrapment and collapse risk
SDADI wooden kitchen step stools can collapse or tip over during use. Children's bodies can also fit through openings on the front and back, creating a risk of entrapment. The company has received reports of eight tip-overs, including four injuries.
- 2026-07-16CPSCDongguan Shinneng Huizheng Network Technology Co., Ltd., dba HurzeinNationwideNoerishia bed rails recalled for entrapment and asphyxiation risk
Noerishia adult portable bed rails (Model KDB-504B) can trap users between the rail and mattress, or within the rail itself, creating a serious risk of asphyxiation and death. The rails also lack required hazard warning labels and do not meet federal safety standards.
- 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
Jobon butane torch lighters do not have the child-resistant safety mechanism required by U.S. law, creating a risk of serious injury or death from fire and burns. The lighters have a side ignition trigger and hands-free operation lock, and come in gray/brown, gold/black, and camouflage print. Approximately 13,200 units were sold online from April 2021 through September 2025.
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