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

2,251 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 DRUG

Skin MD Body Acne Cleanser Recalled Due to Benzene Contamination

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.

Skin MD
Chemical Contamination:
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Camera Over Fall Risk

GE HealthCare recalled 28 dual-head gamma cameras on September 12, 2025. The recall comes after concerns that inadequate support during relocation could lead to a detector fall. This situation poses a high risk of life-threatening injury.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA FOOD

MARS FOODS Recalls Ben's Original Ready Rice Due to Stones

MARS FOODS recalled 1,075 cases of Ben's Original Ready Rice Long Grain & Wild on September 12, 2025. The recall stems from a possible presence of stones in the product. Consumers should not consume the affected rice and seek a refund or replacement.

MARS FOODS
Possible presence
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HIGHFDA DRUG

Major Pharmaceuticals Recalls Chlorpromazine Tablets Over Contamination

Major Pharmaceuticals announced a recall of 1,256 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall stems from the presence of N-Nitroso Desmethyl Chlorpromazine above safe intake levels. Consumers must stop using the product immediately and contact their healthcare provider for guidance.

Chlorpromazine Hydrochloride
CGMP Deviations:
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HIGHFDA DEVICE

Shanghai United Imaging Healthcare Recalls X-ray System Due to Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled two units of its uCT 780 MD Computed Tomography X-ray System on September 12, 2025. Third-party outer covers can trap between the patient table and gantry, causing mechanical interference. This recall affects units distributed in the US and internationally.

UIH Technologies
Third-party outer
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Cameras Over Fall Risk

GE HealthCare recalled 1,386 nuclear medicine gamma cameras on September 12, 2025. Certain models may have been relocated without proper support, risking detector integrity. This could lead to life-threatening injuries from falls.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Camera Over Fall Risk

GE HealthCare recalled three units of the Elscint Helix nuclear medicine gamma camera on September 12, 2025. The recall affects systems that may have been transported without proper support, risking detector falls. This issue poses a high risk of life-threatening injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DRUG

Major Pharmaceuticals Recalls Chlorpromazine Tablets Over Contamination Risk

Major Pharmaceuticals recalled 1,394 blister packs of Chlorpromazine Hydrochloride Tablets due to contamination concerns. The recall occurred on September 12, 2025, after the FDA found N-Nitroso Desmethyl Chlorpromazine above acceptable limits. Consumers should stop using these tablets and seek guidance from healthcare providers.

Chlorpromazine Hydrochloride
CGMP Deviations:
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HIGHFDA DEVICE

UIH Technologies Recalls PET/CT System Over Mechanical Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled four units of its Positron Emission Tomography and Computed Tomography System on September 12, 2025. The recall stems from a risk of mechanical interference during table movement due to third-party outer covers. Healthcare providers and patients must stop using the device immediately.

UIH Technologies
Third-party outer
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HIGHFDA FOOD

Ben's Original Rice Recalled Over Possible Stones Contamination

Ben's Original recalled 273 cases of Ready Rice Original Long Grain White on September 12, 2025. The recall follows concerns about possible stones in the product. Customers in several states, including Texas and California, should not consume the affected rice.

MARS FOODS
Possible presence
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HIGHFDA DEVICE

GE HealthCare Recalls Nuclear Medicine Gamma Cameras Over Fall Risk

GE HealthCare recalled 54 nuclear medicine gamma cameras on September 12, 2025. The recall affects devices that may have been transported without proper detector support. This issue poses a high risk of detector falls, potentially leading to serious injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DEVICE

GE Healthcare Recalls Nuclear Medicine Cameras Due to Fall Risk

GE HealthCare recalled 15 nuclear medicine gamma cameras on September 12, 2025. The recall affects systems that may have been relocated without proper support, risking detector falls. This poses a significant danger of life-threatening injuries to patients and healthcare providers.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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