stop use immediately Recalls

2,229 recalls tagged with “stop use immediately”.

Food & Beverages
HIGH
FDA FOOD

SB FOOD Recalls Gummy Candy Over Unallowed Color Additive

SB FOOD recalled 100 cases of Yoyo Gummy Assorted Flavor on November 21, 2025. The product contains an unapproved color, Carmoisine (E122), posing health risks. Consumers should not consume the candy and seek refunds.

SB FOOD
The products
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Food & Beverages
HIGH
FDA FOOD

Boar's Head Grated Cheese Recalled Due to Listeria Risk

Boar's Head recalled 405 bags of Pecorino Romano Grated cheese on November 21, 2025. The product tested positive for Listeria Monocytogenes, a serious health risk. Consumers should not consume the cheese and seek a refund or replacement immediately.

Boar's Head
Product tested
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Food & Beverages
HIGH
FDA FOOD

Ambriola Grated Pecorino Romano Recalled Due to Listeria Risk

Ambriola Co., Inc. recalled 45 bags of Pinna Grated Pecorino Romano on November 21, 2025, after Listeria Monocytogenes was detected. The recall affects products distributed in 17 states including California and Texas. Consumers should not consume the recalled product and should seek refunds or replacements.

Ambriola Co., Inc.
Product tested
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Food & Beverages
HIGH
FDA FOOD

IKM Aluminum Saucepan Recalled Over Lead Contamination Risk

Lotus Mom Corporation recalled 56 units of its 9-inch aluminum saucepan on November 21, 2025. The product may contain leachable lead, posing serious health risks. Consumers should not use the saucepan and seek refunds immediately.

Lotus Mom Corporation dba Indian Kitchen Mart
Potential contamination
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Oxygen Masks Due to Tubing Disconnect Risk

Medline Industries recalled over 1.6 million oxygen masks on November 21, 2025. The recall affects multiple models after reports of tubing disconnecting during use. This defect can delay patient care and lead to shortness of breath, requiring medical intervention.

Medline Industries, LP
Firm received
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Health & Personal Care
HIGH
FDA DEVICE

Roche Diagnostics Recalling Anti-TSHR Immunoassay Over Diagnosis Risk

Roche Diagnostics Operations recalled 1,300 Anti-TSHR immunoassay cassettes on November 21, 2025. Variability in results may lead to incorrect diagnoses and treatment delays. The recall affects multiple states across the U.S.

Roche Diagnostics Operations
Issues identified:
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Health & Personal Care
HIGH
FDA DRUG

Fagron Compounding Services Recalls Ophthalmic Solution Over Incorrect Formulation

Fagron Compounding Services recalled 2,980 syringes of a topical ophthalmic solution on November 20, 2025. The recall stems from an incorrect product formulation that could pose health risks. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

Fagron Compounding Services
Incorrect Product
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Recalled Spartan Riding Lawn Mower (SRT-XD)
MEDIUM
CPSC

Spartan Mowers Recalls 2025 SRT-XD and KGZ-XD Riding Mowers for Steering Damper Hazard

Spartan Mowers recalled certain Model Year 2025 SRT-XD and KGZ-XD zero-radius-turn riding mowers sold through Spartan dealers nationwide. A steering arm damper can be installed incorrectly, creating a bouncing motion and loss of operator control. Owners should stop using the recalled mowers and contact an authorized Spartan dealer for a free inspection and repair.

Spartan Mowers and UTVs
The riding
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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
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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
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

CareFusion 303 Recalls Automated Dispensing Cabinets Due to Error Risk

CareFusion 303 recalled 53,669 units of Automated Dispensing Cabinets on November 20, 2025. A firmware update caused drawer failures, leading to potential delays in accessing medications. This recall affects devices distributed worldwide, including all U.S. states and several countries.

CareFusion 303
Automated Dispensing
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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
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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
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Health & Personal Care
HIGH
FDA DEVICE

Vortex Surgical Recalls Laser Probe Due to Smooth Passage Issues

Vortex Surgical recalled 221 units of the 25ga Illuminated Flex-Tip Laser Probe on November 19, 2025. The product does not pass through a 25ga cannula smoothly, which poses a high hazard risk. Patients and healthcare providers must stop using the device immediately and follow recall instructions.

Vortex Surgical
Reason for
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Food & Beverages
HIGH
FDA FOOD

Sonex Aluminum Pot Recall: 2 Units for Lead Leaching (2025)

Two Sonex aluminum pots sold in New York are recalled after tests found leachable lead at 0.323 mg/L. The recall is issued by Alanwar Food Corp. Consumers who own the pots should not use them for cooking and should contact Alanwar Food Corp. for refund or replacement information.

Sonex
Products found
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