All Product Recalls

Browse through 2,313 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA FOOD

Ben's Original Rice Recalled Due to Possible Stone Contamination

Ben's Original Ready Rice Whole Grain Brown has been recalled due to potential contamination with stones. The recall affects 315 cases sold in several states including Wisconsin and Texas. Consumers should not consume the product and seek refunds immediately.

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 X-ray System Recalled Due to Mechanical Hazard

Shanghai United Imaging Healthcare Co., Ltd. recalled 22 units of its uCT 550 MD X-ray system on September 12, 2025. The recall was issued after reports that third-party outer covers can trap between the patient table and gantry. This can cause mechanical interference during table movement, posing a high risk to patients and healthcare providers.

UIH Technologies
Third-party outer
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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

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 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

GE HealthCare Recalls Gamma Cameras Due to Fall Hazard

GE HealthCare recalled 102 dual-head nuclear medicine gamma cameras on September 12, 2025. The recall stems from inadequate support during transportation that could lead to a detector fall, posing a life-threatening injury risk. The affected devices are past their End of Guaranteed Service and should not be used immediately.

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 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 Risk

Major Pharmaceuticals recalled 2,064 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall follows the discovery of N-Nitroso Desmethyl Chlorpromazine exceeding safe limits. Consumers must stop using this product immediately and consult healthcare providers for guidance.

Major Pharmaceuticals
CGMP Deviations:
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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 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 DRUG

Major Pharmaceuticals Recalls Chlorpromazine Tablets Over Contaminant Hazard

Major Pharmaceuticals recalled 866 blister packs of Chlorpromazine Hydrochloride Tablets on September 12, 2025. The recall follows the detection of N-Nitroso Desmethyl Chlorpromazine above safe limits. The affected products were distributed nationwide and are classified as a Class II hazard.

Major Pharmaceuticals
CGMP Deviations:
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HIGHFDA DEVICE

GE HealthCare Recalls Gamma Camera Due to Fall Hazard

GE HealthCare recalled 82 units of the Millenium Myosight gamma camera on September 12, 2025. The recall affects systems that may lack sufficient support during transport, posing a risk of detector falls. This defect can result in life-threatening injuries.

GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING
GE HealthCare
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HIGHFDA DEVICE

UIH Technologies Issues Recall for Computed Tomography X-ray System

Shanghai United Imaging Healthcare recalled two units of the uCT ATLAS MD X-ray system on September 12, 2025. The recall follows reports that third-party outer covers can trap between the patient table and gantry, leading to mechanical interference. Healthcare providers and patients must cease use immediately and follow manufacturer instructions.

UIH Technologies
Third-party outer
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