immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalls Shoulder Prosthesis Over Labeling Error

Encore Medical, LP recalled 20 shoulder prosthesis implants on January 15, 2026. Incorrect labeling on the RSP Standard Humeral Socket Insert poses a high hazard risk. Affected products were distributed nationwide across multiple states.

Encore Medical, LP
Knee and
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Health & Personal Care
HIGH
FDA DEVICE

Encore Medical Recalled Humeral Socket Insert Over Labeling Issues

Encore Medical, LP recalled 20 units of its RSP Humeral Socket Insert on January 15, 2026. The recall stems from incorrect labeling on knee and humeral socket implants. Patients and healthcare providers should stop using the device immediately.

Encore Medical, LP
Knee and
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Health & Personal Care
HIGH
FDA DEVICE

Aesculap MINOP TROCAR 150MM Recall for 126 Units in 2026

Aesculap recalls 126 MINOP TROCAR 150MM devices distributed nationwide to U.S. hospitals and clinics after regulators flagged a shaft length issue. The shaft may be longer than specified, potentially harming tissue during procedures. Healthcare facilities should stop using the devices and follow manufacturer recall instructions immediately.

Aesculap
There is
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Recalled RootStim Beard Growth Serum Packaging (Front)
HIGH
CPSC

RootStim Recalls Beard Growth Serum Due to Poisoning Risk

RootStim recalled Beard Growth Serum on January 15, 2026, due to inadequate child-resistant packaging. The product poses a serious poisoning risk to children. Consumers should stop using it immediately and secure it out of reach.

Ronghui Intelligent Manufacturing Technology (Guangzhou) Co., Ltd., of China
The beard
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Recalled Ruahouine Hair Growth Serum
HIGH
CPSC

Ruahouine Hair Growth Serum Recalled Over Child Poisoning Risk

Ruahouine recalled its Hair Growth Serum on January 15, 2026, due to a poisoning hazard. The product lacks child-resistant packaging, violating safety standards. This poses a risk of serious injury or death if ingested by children.

Ruahouine Hair Growth Serum Bottles
The serum
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Recalled HEZI brand power strip (gray)
HIGH
CPSC

HEZI Power Strips Recalled Over Electrocution Risk

HEZI recalled power strips on January 15, 2026, due to an electrocution hazard. The power strips have an ungrounded metal enclosure that can become energized. Consumers should stop using them immediately and seek a refund.

Dongguan Keben Electrical Appliance Co Ltd, of China
The power
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Recalled Asher Pajama Set
HIGH
CPSC

Morgan Lane Recalls Children's Pajama Sets Over Burn Hazard

Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.

Morgan Lane
The recalled
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Recalled R.X.Y Bicycle Helmet
HIGH
CPSC

R.X.Y Bicycle Helmets Recalled for Serious Head Injury Risk

R.X.Y recalled adult bicycle helmets on January 15, 2026, due to safety violations. The helmets fail to meet mandatory impact standards, posing a serious risk of injury or death. Consumers should immediately stop using the helmets and seek a refund.

The recalled
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Recalled BBWOO Baby Lounger in Gray Dinosaur
HIGH
CPSC

BBWOO Baby Loungers Recalled Over Serious Injury Risk

BBWOO recalled baby loungers on January 15, 2026, due to serious injury risks. The loungers violated safety standards, posing entrapment and fall hazards. Consumers should stop using the product immediately and seek a refund.

BBWOO Baby Loungers
The recalled
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Recalled Curtis International Minifridge Model EFMIS121 – serial numbers between A2001 to A2310
HIGH
CPSC

Curtis International Recalls Frigidaire Minifridges Over Fire Risk

Curtis International recalled 50,000 Frigidaire-brand minifridges on January 15, 2026, due to fire and burn hazards. The recall affects model EFMIS121 and previously recalled models EFMIS129, EFMIS137, EFMIS149, and EFMIS175. Consumers should stop using these minifridges immediately and seek a refund.

ShangYu North Electron Manufacture Co. Ltd., of China
The minifridges'
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Recalled Greatale Self-Feeding Pillow
HIGH
CPSC

Greatale Recalls Self-Feeding Pillows Due to Suffocation Risk

Greatale recalled self-feeding pillows on January 15, 2026, due to a serious risk of aspiration and suffocation in infants. The pillows can hold a bottle at an unsafe angle, preventing infants from pulling away. Consumers must stop using the pillows immediately and return them for a full refund.

Greatale
The recalled
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Recalled Adams and StyleWell Adirondack Patio Chair
MEDIUM
CPSC

Adams Manufacturing Recalls Adirondack Chairs Over Injury Risks

Adams Manufacturing recalled Adirondack-style patio chairs on January 15, 2026, due to fall hazards. The chairs can crack and collapse, risking injury to users. The recall affects products sold under the Adams RealComfort and StyleWell brands.

Adams Manufacturing Corp., of Portersville, Pennsylvania
The recalled
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Food & Beverages
HIGH
FDA FOOD

Live it Up Super Greens Recalled Due to Salmonella Contamination

Live it Up brand recalled 795,834 units of Super Greens powder on January 15, 2026, due to possible Salmonella Typhimurium contamination. The affected products are sold nationwide, including Puerto Rico and Guam. Consumers should not consume the product and seek refunds immediately.

SUPERFOODS
Products may
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Food & Beverages
HIGH
FDA FOOD

Live it Up Super Greens Recall Due to Salmonella Contamination

Superfoods, Inc. recalled 795,834 units of Live it Up brand Super Greens on January 15, 2026. The dietary supplement may be contaminated with Salmonella Typhimurium, posing a health risk. Consumers should stop using the product immediately and seek a refund or replacement.

SUPERFOODS
Products may
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Health & Personal Care
HIGH
FDA DRUG

Greenstone Recalls Methylprednisolone Tablets Due to Dosing Error

Greenstone LLC recalled 3,456 cartons of methylprednisolone tablets on January 15, 2026. The recall follows reports of incorrect dosing information due to misapplied blister foil. Consumers should stop using the product immediately and contact their healthcare provider.

METHYLPREDNISOLONE
Labeling: Not
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Food & Beverages
HIGH
FDA FOOD

Aonic Complete Hers Dietary Supplement Recalled for Contamination Risk

Aonic Inc. recalled 3,630 bottles of Aonic Complete Hers dietary supplement on January 15, 2026. Possible contamination with coliforms, E. coli, and Pseudomonas aeruginosa prompted the recall. Consumers in Utah should stop using the product immediately.

TKS Co-pack Manufacturing
Possible coliforms,
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Food & Beverages
HIGH
FDA FOOD

Aonic Complete Dietary Supplement Recalled for Contamination Risk

Aonic Inc. recalled 780 bottles of its Complete dietary supplement on January 15, 2026, due to potential contamination with E. coli and Pseudomonas aeruginosa. Consumers in Utah should stop using the product immediately and seek refunds or replacements. The recall affects specific lots with expiration dates of December 27, 2026.

TKS Co-pack Manufacturing
Possible coliforms,
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