cpsc regulated Recalls

2,056 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Baby Soothe Herbal Supplement Over Misbranding

A New Life Herbs recalled 49 bottles of Baby Soothe Herbal Supplement on November 20, 2025. The product misbrands due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

A New Life Herbs
Unapproved drug
Read more
Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Sinus Cap Herbal Supplement Over Misbranding

A New Life Herbs recalled Sinus Cap Herbal Supplement on November 20, 2025, due to unapproved drug claims. The product lacks a Supplement Facts label, which misbrands it. Consumers should not consume the product and seek refunds or replacements.

A New Life Herbs
Unapproved drug
Read more
Recalled Play Yard
HIGH
CPSC

Anna Queen Play Yard Recall 2025 for Suffocation Risk on Amazon

Anna Queen recalls Play Yards sold on Amazon due to suffocation and entrapment risks. The product features black fabric sides, gray mesh panels, and white top rails with a bear-print design. Model P700 and production date 202503 appear on packaging and a removable tag. Consumers should stop using recalled units and obtain a full refund from Anna Queen.

Play Yards
The play
Read more
Health & Personal Care
HIGH
FDA FOOD

A New Life Herbs Recalls Ear Drops Over Misbranding Issues

A New Life Herbs, LLC recalled 22 bottles of Mullein flower alcohol tincture on November 20, 2025. The product is misbranded due to unapproved drug claims and lack of a Supplement Facts label. Consumers should stop using this product immediately.

A New Life Herbs
Unapproved drug
Read more
Recalled Anzmtosn Magnet Fidget Spinner Set
HIGH
CPSC

Anzmtosn 15-Piece Magnet Fidget Spinner Sets Recalled for Ingestion Risk (2025)

Anzmtosn recalled 15-piece Magnet Fidget Spinner Sets sold on Amazon after magnets pose a serious ingestion hazard. The magnets can detach and, if swallowed, attract each other or metal objects and cause internal injuries. Stop using the sets now and email disposal photos to Anzmtosn53@163.com for a full refund.

Anzmtosn
The recalled
Read more
Recalled MoonSoll Ethanol Fuel Bottle
HIGH
CPSC

Demlar Recalls MoonSoll and Magic Chems Fuel Bottles Over Flash Fire Risk (2025)

Demlar recalled MoonSoll ethanol and Magic Chems bioethanol fuel bottles sold online by the Demlar Online Store. The bottles lack flame mitigation devices required by the Portable Fuel Container Safety Act, creating a flash-fire risk. Consumers should stop using the recalled bottles immediately and contact Demlar for a full refund.

Demlar
The ethanol
Read more
Recalled Bearlala Baby Lounger Top View
HIGH
CPSC

Bearlala Baby Loungers Recalled Over Entrapment and Fall Hazards (2025)

Bearlala baby loungers sold on Walmart.com by Nuoxuann are recalled. The recall cites a violation of the mandatory Infant Sleep Products standard. The loungers have sides that are too low and foot openings that are wider than allowed, creating fall and entrapment hazards. Consumers should stop using the loungers immediately and contact Nuoxuann for a full refund.

Bearlala
The recalled
Read more
Recalled 4-in-1 Baby Stroller - Black
MEDIUM
CPSC

AliExpress Recalls Convertible Strollers for Fall Hazard 2025

AliExpress recalls a convertible stroller sold online from September 2024 through October 2025 for $215 to $415. The restraint system can fail, creating a fall hazard that could cause serious injury or death. Stop using the stroller now and contact AliExpress for a full refund; you must cut the restraints and email a photo of the destroyed product.

AliExpress
The stroller
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medtronic Recalls Clinician Programmer App Over High-Risk Software Issue

Medtronic Neuromodulation recalled 7,667 Clinician Programmer Applications on November 20, 2025. A software issue may prevent patients from resuming therapy, leading to a recurrence of pain symptoms. Affected models include A71100 and associated tablets.

Medtronic Neuromodulation
Software issue
Read more
Food & Beverages
HIGH
FDA FOOD

GUSTO GROUP Recalls Shrimp Paste Over High Lead Levels

GUSTO GROUP, INC. recalled 7 cases of Shrimp Paste (Klong Kone) 'M' due to high lead levels. The recall affects products distributed in Iowa and New Jersey. Consumers should not consume the product and seek refunds immediately.

GUSTO GROUP
Product tested
Read more
Health & Personal Care
HIGH
FDA DEVICE

Steris Washers Recalled Due to Electrical Arcing Hazard

Steris recalled 22 AMSCO 7053HP Washer/Disinfectors on November 19, 2025, due to a risk of electrical arcing. The issue arises from a wire connected to the electrical box that may shift from its intended position. Users must stop using the device immediately and follow recall instructions.

Steris
Wire connected
Read more
Food & Beverages
HIGH
FDA FOOD

New Way Import Recalls Mustard Over Undeclared Wheat Allergen

New Way Import Inc recalled preserved mustard on November 19, 2025, due to undeclared wheat allergens. The product, sold in predominantly green packaging with black Chinese lettering, poses a high risk to consumers with wheat allergies. Approximately 55 cases of the product were distributed to 23 retail locations in California.

NEW WAY IMPORT
Undeclared allergen
Read more
Health & Personal Care
HIGH
FDA DEVICE

Steris Recalls AMSCO 7052HP Washer/Disinfector Due to Fire Hazard

Steris recalled the AMSCO 7052HP Washer/Disinfector on November 19, 2025, after reports of electrical arcing. The issue results from a wire potentially shifting out of position, posing a fire risk. No injuries or shocks have been reported.

Steris
Wire connected
Read more
Food & Beverages
HIGH
FDA FOOD

Karabetian Import and Distribution Recalls Frozen Kunefe for PHOs

Karabetian Import and Distribution recalled 338 boxes of Zimi Kunefe on November 18, 2025, due to partially hydrogenated oils. The recall affects frozen dessert products distributed in nine states including California and Texas.

Karabetian Import and Distribution
partially hydrogenated
Read more
Health & Personal Care
HIGH
FDA DEVICE

AGFA Recalls Digital Radiography X-Ray System Over Radiation Risk

AGFA Healthcare recalled 35 Digital Radiography X-Ray systems on November 18, 2025, due to a risk of exceeding safe radiation levels. The recall affects systems distributed nationwide in the U.S. Users must stop using the device immediately and follow manufacturer instructions.

AGFA Healthcare
It is
Read more