These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

1,488 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
HIGHFDA DRUG

Cipla USA Recalls Cinacalcet Hydrochloride Tablets Over Nitrosamine Hazard

Cipla USA, Inc. recalled 15,744 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall follows the discovery of a nitrosamine impurity exceeding acceptable daily intake limits. Consumers should stop using the product immediately and consult healthcare providers.

CINACALCET
CGMP Deviations:
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HIGHFDA DRUG

Cipla Recalls Cinacalcet Hydrochloride Tablets Over Impurity Risk

Cipla USA, Inc. recalled 63,504 bottles of Cinacalcet Hydrochloride Tablets on November 14, 2025. The recall results from a nitrosamine impurity, N-nitroso-cinacalcet, exceeding acceptable daily intake limits. Consumers should stop using the tablets immediately and contact healthcare providers for guidance.

CINACALCET
CGMP Deviations:
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Recalled Zigjoy Toddler Sleep Sack with Feet – Excavator print
HIGH
CPSC

Zigjoy Recalls Children's Sleep Sacks Due to Burn Hazard

Zigjoy recalled children's sleep sacks on November 13, 2025, after discovering a violation of mandatory flammability standards. The recall affects sleep sacks sold in blue and pink, posing a serious burn risk to children. Consumers should stop using the sleep sacks immediately and contact Zigjoy for a refund.

Zigjoy Sleep Sacks with Feet
The recalled
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Recalled CR2032 Lithium Coin Batteries, Item 00263
HIGH
CPSC

Great Lakes Select Battery Packs Recalled Over Ingestion Risk

Great Lakes Wholesale International recalled select battery packs on November 13, 2025. The battery packs lack child-resistant packaging and pose a serious ingestion risk for children. Consumers should stop using the products immediately and seek refunds.

Great Lakes Wholesale International
The button
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Recalled Bettina Doll Set with Magic Light Unicorn
HIGH
CPSC

Bettina Doll Sets Recalled Due to Battery Ingestion Hazard

Bettina Doll Sets with Magic Light Unicorn recalled on November 13, 2025, after reports of battery ingestion risks. The unicorn's battery compartment is accessible to children. The recall affects all units sold on Amazon by Shantou Chenghai Xingzigu Toy Industry.

Bettina Doll Sets
The doll
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Recalled MMA008 Portable Wireless Charging Stand
HIGH
CPSC

Belkin Recalls Power Banks and Charging Stands Over Fire Hazards

Belkin recalled portable power banks and charging stands on November 13, 2025, due to fire and burn hazards. Models MMA008, BPB002, and PB0003 are affected. Consumers should stop using these products immediately and return them for a refund.

Belkin International Inc., of El Segundo, California
The lithium-ion
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Recalled Powerwall 2 AC Battery System
HIGH
CPSC

Tesla Recalls Powerwall 2 Batteries Due to Fire Risk

Tesla recalled certain Powerwall 2 battery systems on November 13, 2025, due to fire and burn hazards. The recall affects units sold from November 2020 through December 2022. Consumers must stop using the units immediately to prevent serious injury or death.

Tesla, Inc., of Reno, Nevada
The lithium-ion
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HIGHFDA FOOD

Jeni's Ice Cream Bars Recalled Due to Undeclared Allergens

Jeni's Splendid Ice Creams recalled 3,767 cases of Passion Fruit Dreamsicle Ice Cream Bars on November 13, 2025. The bars contain undeclared allergens, wheat and soy. Consumers should not consume the product and seek refunds.

Jeni's Splendid Ice Creams
Undeclared allergens
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HIGHFDA FOOD

American Nuts Recalls Macadamia Nuts Over Salmonella Risk

American Nuts, LLC recalled 2,700 units of dry roasted macadamia nuts on November 13, 2025, due to potential Salmonella contamination. The affected product is sold in 20-ounce packages and was distributed in Hawaii. Consumers should not consume the product and seek a refund.

American Nuts
Potential Salmonella
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HIGHNHTSA

Nissan Recalls 2025 Kicks Over Rollaway Risk

Nissan North America recalled certain 2025 Kicks vehicles on November 12, 2025, due to a malfunctioning "Shift-to-Park" warning. The issue may lead to unexpected vehicle movement when the ignition is shut off while not in park, posing a rollaway risk. Owners will receive notification letters with further instructions, including a free fix.

Nissan
When the
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HIGHFDA DRUG

Walgreens Saline Nasal Spray Recalled Due to Microbial Contamination

Walgreens recalled 41,328 bottles of Saline Nasal Spray on November 12, 2025. The recall follows a discovery of microbial contamination by pseudomonas lactis. Consumers should stop using the product immediately and seek guidance from healthcare providers.

Medical Products Laboratories
Microbial contamination
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HIGHFDA DEVICE

Cardinal Health Recalls ChemoPlus Gowns Over Expiration Date Error

Cardinal Health 200 recalled 251,165 ChemoPlus gowns on November 12, 2025, due to incorrect expiration dates. The gowns are mislabeled with a five-year shelf life instead of the correct three years. Patients and healthcare providers must stop using these gowns immediately.

Cardinal Health 200
Affected gowns
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HIGHFDA FOOD

Genepro Protein Powder Recalled for Mislabeling Risk

Genepro Protein, Inc. recalled 250 bags of Genepro Whey 4th Generation Plasma Treated Protein on November 12, 2025. The product is mislabeled and fails to declare milk as an allergen, posing a serious risk to consumers with dairy allergies. The affected product has a 'Best By' date of February 13, 2027.

Genepro Protein
Product is
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HIGHFDA FOOD

Stuffed Foods Recalls Cacio e Pepe Arancini Over Soy Allergy Risk

Stuffed Foods recalled 51 cases of Cacio e Pepe Arancini on November 12, 2025. The products contain undeclared soy protein concentrate, posing a risk to those with soy allergies. The affected items were distributed in Connecticut, Massachusetts, Florida, and Missouri.

Stuffed Foods
Undeclared Soy
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HIGHFDA DEVICE

Stryker Recalls CranialMask Tracker Due to Device Error

Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.

Howmedica Osteonics
When the
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