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
Health & Personal Care
HIGH
FDA DRUG

Walgreens Saline Nasal Spray With Xylitol Recalled for Microbial Contamination (41,328 Bottles, 2025

Walgreens Saline Nasal Spray With Xylitol, distributed by Walgreens Co., is recalled nationwide. The product was found with microbial contamination, specifically Pseudomonas lactis, in a non-sterile formulation. Consumers should stop using the product immediately and contact Medical Products Laboratories, Inc. for guidance or consult a clinician.

Medical Products Laboratories
Microbial contamination
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Health & Personal Care
HIGH
FDA DEVICE

Cardinal Health Recalls ChemoPlus Gowns Over Expiration Date Error

Cardinal Health 200 recalled 251,165 ChemoPlus gowns on November 12, 2025, due to incorrect expiration dates. The gowns are mislabeled with a five-year shelf life instead of the correct three years. Patients and healthcare providers must stop using these gowns immediately.

Cardinal Health 200
Affected gowns
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Food & Beverages
HIGH
FDA FOOD

Santos Agency Recalls Brass Langri Cookware Over Lead Risk

Santos Agency recalled Brass Langri Cookware on November 12, 2025, due to potential lead contamination. Consumers should not use the product and seek a refund. The affected item features sticker label: 14.

Santos Agency
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Stuffed Foods Recalls Cacio e Pepe Arancini Over Soy Allergy Risk

Stuffed Foods recalled 51 cases of Cacio e Pepe Arancini on November 12, 2025. The products contain undeclared soy protein concentrate, posing a risk to those with soy allergies. The affected items were distributed in Connecticut, Massachusetts, Florida, and Missouri.

Stuffed Foods
Undeclared Soy
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Health & Personal Care
HIGH
FDA DEVICE

Stryker Recalls CranialMask Tracker Due to Device Error

Stryker recalled 320 units of the CranialMask Tracker on November 12, 2025, due to software errors during surgery. The device fails to activate properly, displaying an error message that prevents its use. Healthcare providers must stop using this device and follow recall instructions immediately.

Howmedica Osteonics
When the
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Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breakage Risk

Olympus Corporation recalled 29 units of its Resection Sheath on November 11, 2025. The recall affects model numbers A22014A and A22014T due to complaints of the ceramic tip breaking. The company advises immediate cessation of use and adherence to recall instructions.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Tips

Olympus Corporation of the Americas recalled 1,676 units of Resection Sheath Model No. A22042A on November 11, 2025. Complaints indicated the ceramic tip of the sheath could break during use, posing a hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

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

Olympus Resection Sheath Recalled Due to Breakage Hazard

Olympus Corporation of the Americas recalled the Resection Sheath Model A2666T on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard for patients. Healthcare providers and patients should stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Recalls Endoscopic Sheath Due to Breakage Risk

Olympus Corporation of the Americas recalled 91 units of the Inner Sheath Model No. A4741 on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

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

Olympus Resection Sheath Recalled Due to Ceramic Tip Breakage

Olympus Corporation recalled 899 units of the Resection Sheath Model No. A42011A on November 11, 2025. Complaints indicate that the ceramic tip may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Ceramic Tip Breaking

Olympus Corporation of the Americas recalled 1,634 units of the A22042T Resection Sheath on November 11, 2025. The recall follows complaints of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Hazard

Olympus Corporation of the Americas recalled 207 units of its Resection Sheath, Model No. A22043T, on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a serious hazard. Patients and healthcare providers must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Tip Hazard

Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

AVID Medical Recalls Halyard MINI PLUS KIT SOUTH Over Transplant Risk

AVID Medical recalled 380 units of the Halyard MINI PLUS KIT SOUTH on November 11, 2025. The devices are unsuitable for organ transplant procedures, posing potential health risks. Healthcare providers and patients must stop using the device immediately.

AVID Medical
Devices are
Read more
Health & Personal Care
HIGH
FDA DEVICE

AVID Medical Recalls Organ Recovery Kit Due to Unsuitability

AVID Medical recalled 52 units of the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, on November 11, 2025. The devices are unsuitable for organ transplant procedures, presenting a serious health risk. Healthcare providers must stop using the device immediately and follow recall instructions.

AVID Medical
Devices are
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls DEXLOCK Achilles Repair Implant Kits Due to Surgical Risk

Medline Industries recalled 163 DEXLOCK Achilles Repair Implant Kits on November 11, 2025, due to a potential hazard. Users reported drill bits fusing to the drill guide, which may prolong surgical procedures. The recall affects kits distributed nationwide in multiple states.

Medline Industries, LP
There have
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Health & Personal Care
HIGH
FDA DRUG

Dr. Reddy's Labs Recalls Varenicline Tablets Over Potency Issues

Dr. Reddy's Laboratories recalled 4,800 bottles of Varenicline tablets on November 11, 2025, due to sub potent drug levels. The affected lot failed stability tests, posing potential health risks to users. Consumers should stop using the product immediately and consult healthcare providers.

VARENICLINE TARTRATE
Sub potent
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Health & Personal Care
HIGH
FDA DEVICE

AVID Medical Recalls Organ Recovery Kit Due to Unsuitability

AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

AVID Medical
Devices are
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Inner Sheath Recalled Due to Breakage Risk

Olympus Corporation of the Americas recalled the Inner Sheath 21 Fr., Model No. A2660T, on November 11, 2025. The recall follows reports of the ceramic tip breaking during use. Patients and healthcare providers should stop using the device immediately.

Olympus Corporation of the Americas
Complaints of
Read more
Health & Personal Care
HIGH
FDA DEVICE

Olympus Resection Sheath Recalled Due to Breaking Ceramic Tip

Olympus Corporation of the Americas recalled 3,484 units of the Resection Sheath Model No. A22041A on November 11, 2025. Reports indicate the ceramic tip of the device may break during use, posing a serious hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.

Olympus Corporation of the Americas
Complaints of
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