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

3,615 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
Food & Beverages
HIGH
FDA FOOD

Palmetto Gourmet Foods Vegetarian Chicken Flavor Ramen Recalled for Yellow #5 (5,664,960 Units, 2026

Palmetto Gourmet Foods recalled 5,664,960 three-ounce packages of Vegetarian Chicken Flavor Ramen sold at multiple retailers nationwide after undeclared Yellow #5 was detected. The recall covers products with a Best By Date before 01/15/2027. Consumers should not eat this product and should contact Palmetto Gourmet Foods for refund or replacement information by mail.

Palmetto Gourmet Foods
Product contains
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Health & Personal Care
HIGH
FDA DEVICE

CVS Wound Care Device Recalled Due to Sterile Barrier Breach

CVS recalled 2,906 units of its wound care device on January 16, 2026. The recall stems from potential packaging failures that may compromise sterility. Affected products include model number CVS405406, distributed across multiple states and internationally.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls Medical Dressing Due to Sterility Risk

Integra LifeSciences Corp. recalled 55,276 units of MEDIHONEY Calcium Alginate with Active Leptospermum Honey on January 16, 2026. The recall cites potential packaging failures that may compromise sterility. Affected products include model numbers 31012, 31022, and 31045.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Software Hazard

Olympus Corporation recalled 18 High Flow Insufflation Units on January 16, 2026, due to a software issue that can cause overpressure events. The recall affects model number UHI, which is used for laparoscopic procedures. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

GE Healthcare
Under certain
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Over Software Malfunction

Olympus Corporation recalled 485 units of the High Flow Insufflation Unit, Model UHI-3, on January 16, 2026. The recall follows reports of a software algorithm issue that may cause overpressure events. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DEVICE

Integra LifeSciences Recalls MediHoney Gel for Packaging Issues

Integra LifeSciences Corp. recalled 49,367 units of MediHoney Gel on January 16, 2026. The recall follows potential packaging failures that may compromise the sterile barrier. Affected products include model numbers 31805 and 31815, distributed worldwide.

Integra LifeSciences Corp.
Potential packaging
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Insufflation Unit Recalled Due to Overpressure Hazard

Olympus Corporation recalled 744 High Flow Insufflation Units on January 16, 2026. A software algorithm issue may lead to overpressure events during use. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Issue with
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Health & Personal Care
HIGH
FDA DRUG

Specialty Process Labs Issues Recall for Subpotent Thyroid Drug

Specialty Process Labs recalled 58 grams of Thyroid, USP due to subpotency. The recall affects products distributed nationwide. Consumers should stop using the drug immediately and contact their healthcare provider.

Specialty Process Labs
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

Bader Enterprises Recalls Premium Food Jordan Almonds in 2.0 oz & 3.5 oz Packaging (2026 Recall)

Bader Enterprises recalls 60 pounds of Premium Food Jordan Almonds sold in New Jersey and New York. The product contains undeclared wheat and blue color additives. Consumers who purchased the product should not consume it. Contact Bader Enterprises for refund or replacement information via two or more notification methods.

Bader Enterprises
Contains undeclared
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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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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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