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

2,247 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
HIGHFDA DEVICE

B BRAUN MEDICAL Recalls Hemodialysis Bloodlines Over Air Bubble Risk

B BRAUN MEDICAL recalled 1,298,454 hemodialysis bloodlines on September 30, 2025. The recall results from the risk of micro-air bubbles due to damaged connectors. Patients should stop using the product immediately and follow the manufacturer’s instructions.

B BRAUN MEDICAL
The potential
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HIGHFDA DEVICE

Philips Medical Systems Recalls Zenition 50 X-Ray Systems Due to Imaging Issues

Philips Medical Systems Nederland B.V. recalled 29 Zenition 50 x-ray systems on September 29, 2025. The devices may suffer from corrosion of the Image Intensifier Television control board, leading to poor image quality. Users must stop using the device immediately and follow the recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Over time
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HIGHFDA DRUG

Acuity Specialty Products Recalls Hand Sanitizer Due to Methanol Risk

Acuity Specialty Products recalled its Wyandotte Sanifect E3 hand sanitizer on September 29, 2025. The recall affects multiple package configurations due to potential methanol contamination. Consumers should stop using the product immediately and contact the company for guidance.

Acuity Specialty Products
cGMP deviations:
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HIGHFDA DRUG

AFCO Hand Sanitizer Recalled Due to Methanol Risk

AFCO recalled hand sanitizer on September 29, 2025, due to a risk of methanol contamination. The company failed to conduct required testing on incoming alcohol components. Consumers should stop using the product immediately.

AFCO
cGMP deviations:
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HIGHFDA DRUG

Medline Recalls Alcohol Prep Pads Due to Subpotency Risk

Medline Industries recalled 222,800 boxes of alcohol prep pads on September 29, 2025. The recall follows concerns the product may not meet potency standards. Consumers must stop using the pads and seek guidance from healthcare providers.

Medline Industries, LP
Subpotent Drug
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HIGHFDA FOOD

New Age International Recalls Enoki Mushroom Over Listeria Risk

New Age International, Inc. recalled 175 boxes of its Signature brand Enoki Mushroom on September 29, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not eat the product and seek a refund or replacement.

New Age International
Product may
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HIGHFDA FOOD

Wegmans Cheesecake Recalled Due to Undeclared Pecan Hazard

Wegmans recalled 2,216 units of Ultimate Plain Cheesecake on September 29, 2025. The product contains undeclared pecans, posing a serious allergy risk. Customers in Pennsylvania and Virginia should not consume this item.

Eli's Cheesecake
undeclared pecan
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HIGHFDA FOOD

Vicky IT Recalls Bona Fish Due to Botulism Risk

Vicky IT Inc. recalled 10 lbs of Bona Fish on September 27, 2025. The product poses a high risk of contamination with Clostridia botulinum, mold, and filth. Consumers should not eat the fish and seek refunds immediately.

Vicky IT
Fish is
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HIGHFDA FOOD

Albertsons Recalls Pasta Salad Due to Listeria Contamination

Albertsons Companies recalled Basil Pesto Bowtie Pasta Salad on September 26, 2025. The product may contain Listeria monocytogenes, a serious foodborne pathogen. The recall affects products sold under multiple store banners in several states.

Albertsons Companies
Listeria monocytogenes.
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HIGHFDA DRUG

Dr. Reddy's Laboratories Recalled Succinylcholine Injection Over Safety Concerns

Dr. Reddy's Laboratories recalled 571 vials of Succinylcholine Chloride Injection on September 26, 2025. The recall stems from out-of-specification results during stability testing, indicating a decreased preservative concentration. The product is used for intravenous or intramuscular administration and is available by prescription only.

SUCCINYLCHOLINE
Out-of-Specification (OOS)
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HIGHFDA FOOD

Wholesale Produce Supply Recalls Fresh Fruit Mix Over Listeria Risk

Wholesale Produce Supply LLC recalled 307 cases of fresh fruit mix on September 26, 2025. The recall follows potential contamination with Listeria monocytogenes. The affected products include cantaloupe, honeydew, and red grapes packaged under various brand names.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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HIGHFDA FOOD

MAYEJ COMERCIALIZADORA Recalls Italian Parsley Due to Pathogen Risk

MAYEJ COMERCIALIZADORA S. de R.L. de C.V. recalled 1,288 boxes of Italian Parsley on September 26, 2025. The recall follows concerns over contamination with Cyclospora cayetanensis, a harmful pathogen. Consumers should avoid consumption and seek refunds immediately.

MAYEJ COMERCIALIZADORA S. de R.L. de C.V.
pathogen Cyclospora
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HIGHFDA FOOD

Wholesale Produce Supply Recalls Cantaloupe Chunks Over Listeria Risk

Wholesale Produce Supply LLC recalled 307 cases of cut cantaloupe chunks on September 26, 2025. The recall affects products sold under the Fresh & Finest and Harvest Cuts brands due to potential Listeria monocytogenes contamination. Consumers should not eat these products and seek refunds immediately.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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HIGHFDA FOOD

WPS Recalls Cut Fresh Fruit Tray Over Listeria Risk

Wholesale Produce Supply LLC recalled 307 cases of cut fresh fruit trays on September 26, 2025. The recall follows potential Listeria monocytogenes contamination. The affected trays were distributed in Iowa, Illinois, North Dakota, Nebraska, and Wisconsin.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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HIGHFDA FOOD

Wholesale Produce Supply Recalls Fresh Cut Fruit Over Listeria Risk

Wholesale Produce Supply LLC recalled 307 cases of fresh cut fruit on September 26, 2025. The recall includes cantaloupe, honeydew, pineapple, and red grapes due to potential Listeria monocytogenes contamination. Consumers should not consume the product and seek a refund or replacement.

WHOLESALE PRODUCE SUPPLY LLC
Potential Listeria
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HIGHFDA FOOD

Kroger Recalls Basil Pesto Bowtie Pasta Salad Over Listeria Risk

Kroger recalled 5,567.4 pounds of Basil Pesto Bowtie Pasta Salad on September 26, 2025. The salad contains a pasta ingredient linked to potential Listeria monocytogenes contamination. Affected products were sold in various states across the U.S.

The Kroger Co
Store-made deli
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HIGHFDA FOOD

Wegmans Cheesecake Recalled for Undeclared Pecans Risk

Wegmans recalled 521 units of its Large Ultimate Strawberry Topped Cheesecake on September 26, 2025. The product contains undeclared pecans, posing a serious risk to those with nut allergies. The cheesecake was sold across Virginia, Maryland, North Carolina, and Washington D.C.

Wegmans Food Markets
Contains undeclared
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