adult product Recalls

989 recalls tagged with “adult product”.

Recalled KingPavonini Adult Portable Bed Rail Model BC-CBJ-X
HIGH
CPSC

KingPavonini Recalls 6 Adult Portable Bed Rails Over Entrapment Risk (2025 Recall)

KingPavonini recalled six adult portable bed rails sold on Amazon after determining the product poses a risk of serious injury or death from entrapment and asphyxiation. The recall cites a failure to meet mandatory standards and missing hazard warning labels. Consumers should stop using the recalled bed rails immediately and contact KingPavonini for a refund or free replacement.

KingPavonini
The recalled
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Recalled Vivohome Adult Portable Bed Rail - Model VH1316-WC
HIGH
CPSC

Vivohome Recalls Adult Portable Bed Rails for Entrapment Hazard in 2025

Vivohome recalled adult portable bed rails due to a risk of entrapment and asphyxiation. The recall covers models VH1316-WC and VH1316-WH. The rails measure about 36.6 inches long, 16.1 inches wide and 15.7 inches high and have a wooden or metallic top bar with a red release button that can collapse. Stop using the recalled rails and contact Vivohome for a full refund.

Vivohome
The recalled
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Recalled Outdoor Master children's helmet - model OM-TD BIKE
HIGH
CPSC

Outdoor Master OM-TD BIKE and OM-KSKB Helmets Recalled for Head Injury Risk (2025)

Outdoor Master recalled two helmet models sold and imported by Outdoor Master after a risk of serious head injury. The recall covers OM-TD BIKE and OM-KSKB helmets. The recall cites noncompliance with positional stability and coverage requirements. Stop using the recalled helmets and contact Outdoor Master for a full refund.

Outdoor Master
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Electric Homecare Beds Due to Fire Hazard

Medline Industries recalled 138,412 electric homecare beds on November 26, 2025. Hazardous hand control pendants may overheat and pose a fire risk. The recall follows 58 reports of sparking, burning, and smoking incidents.

Medline Industries, LP
Medline Industries
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Food & Beverages
HIGH
FDA FOOD

Imu-Tek Colostrum Powder Recalled Due to Undeclared Allergen

Imu-Tek Animal Health recalled 113 bottles of Immuno-5 Colostrum Powder on November 25, 2025. The product contains an undeclared milk allergen, posing a risk to consumers with milk allergies. The recall affects states including CA, TX, and FL.

Imu-Tek Animal Health
Undeclared milk
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Health & Personal Care
HIGH
FDA DRUG

Duloxetine Capsules Recalled Over High N-Nitroso Impurity Risk

Towa Pharmaceuticals recalled 3,397 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations resulting in N-nitroso-duloxetine levels exceeding FDA limits. Consumers must stop using the product immediately.

DULOXETINE
CGMP Deviations;
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Health & Personal Care
HIGH
FDA DEVICE

Abbott Recalls FreeStyle Libre 3 Plus Sensor Over Glucose Errors

Abbott Diabetes Care recalled 8,062 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may cause inaccurate low glucose readings, posing serious health risks. Consumers should stop using the device immediately and follow recall instructions.

Abbott Diabetes Care
Due to
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Food & Beverages
HIGH
FDA FOOD

Gimme Coffee Recalls Pods Over Undeclared Caffeine Hazard

Gimme Coffee, Inc. recalled 252 boxes of Decaf de Agua coffee pods on November 24, 2025. The product contains undeclared caffeine, posing a risk to consumers sensitive to caffeine. Affected products include those with best-by dates of September 30, 2025, and October 15, 2025.

Gimme Coffee
Undeclared caffeine
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Health & Personal Care
HIGH
FDA DEVICE

Abbott Recalls FreeStyle Libre 3 Plus Sensors Over Low Glucose Risk

Abbott Diabetes Care recalled 1,663,241 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may lead to incorrect low glucose results, creating serious health risks for users. Patients should stop using the sensors immediately and follow recall instructions.

Abbott Diabetes Care
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Changchun Wancheng Recalls Male Fertility Test Over False Results

Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.

Changchun Wancheng Bio-Electron Co.
Test strips
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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

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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Food & Beverages
HIGH
FDA FOOD

A New Life Herbs Recalls Herbal Supplement Over Misbranding Issues

A New Life Herbs, LLC recalled 116 bottles of its anti-virus herbal supplement on November 20, 2025. The product misbranded due to unapproved drug claims and missing Supplement Facts label. Consumers should stop using the product immediately and seek a refund.

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

A New Life Herbs Recalls Baby Allergy Herbal Supplement Over Label Issues

A New Life Herbs, LLC recalled 23 bottles of its Baby Allergy Herbal Supplement on November 20, 2025. The recall follows unapproved drug claims and absence of a Supplement Facts label on the product. Consumers should not consume the supplement and should seek refunds immediately.

A New Life Herbs
Unapproved drug
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Health & Personal Care
HIGH
FDA 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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Food & Beverages
HIGH
FDA FOOD

Face Rock Creamery Vampire Slayer Garlic Cheddar 6 oz Recalled for Listeria Risk (2025)

Face Rock Creamery recalled 16 units of Vampire Slayer Garlic Cheddar Cheese, 6 oz, distributed in Oregon after an FDA environmental sample detected Listeria monocytogenes in the packaging area. The hazard is a contamination risk that could cause life-threatening infection in some populations. Consumers should not eat the cheese and should contact Face Rock Creamery for a refund or replacement.

Face Rock Creamery
FDA environmental
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Health & Personal Care
HIGH
FDA 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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