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.

Immediate attention

High Risk Recalls

3,598 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
High-risk recalls
3,598
Action level
Stop use

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
Health & Personal Care
HIGH
FDA DRUG

Agebox iKids-Growth Capsules Recalled Over Undeclared Ingredient

AGEBOX Inc. recalled 665 bottles of iKids-Growth capsules on October 28, 2025, due to undeclared ibutamoren. The product was marketed without an approved NDA/ANDA. Consumers should stop using the product immediately and contact Agebox for guidance.

Agebox
Marketed Without
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Adhesive Bandages Due to Sterility Concerns

Medline recalled 4.4 million Quick Strip Plastic Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals compromising sterility. Consumers and healthcare providers should stop using these bandages immediately.

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Adhesive Bandages Over Sterility Concerns

Medline Industries recalled 11,291,800 units of Quick Strip Fabric Sterile Adhesive Bandages on October 27, 2025. The recall affects all lots due to potential open seals that compromise sterility. Consumers should stop using these bandages immediately.

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls Curad Bandages Due to Sterility Risk

Medline has identified that all lots of the Curad Touch-Free and Quick-Strip Bandages may exhibit open seals in the packaging which may compromise the sterility of the product.

Medline Industries, LP
Medline has
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Health & Personal Care
HIGH
FDA DRUG

Cipla USA Recalls Lanthanum Carbonate Tablets Over Stability Issues

Cipla USA recalled 1,180 boxes of Lanthanum Carbonate chewable tablets on October 24, 2025. The recall follows a failure to meet stability specifications for hardness tests. Consumers and healthcare providers must stop using the product immediately.

LANTHANUM CARBONATE
Failed stability
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Health & Personal Care
HIGH
FDA DEVICE

EDAN Patient Monitors Recalled Due to Cybersecurity Risks

EDAN recalled 379 patient monitors on October 24, 2025, due to potential cybersecurity issues. Models iX10, iX12, and iX15 pose risks to patient safety. Healthcare providers should stop using these devices immediately.

Edan Diagnostics
As a
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