All Product Recalls

Browse through 2,234 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Over Metal Contamination

Asteria Health recalled 24,099 Estradiol, 10 mg pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately. The recall affects pellets distributed nationwide in the USA.

F.H. INVESTMENTS, Inc.
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HIGHFDA FOOD

Beacon Promotions Recalls M&Ms Peanut Candies Over Allergen Risk

Beacon Promotions recalled 541 units of repackaged M&Ms Peanut candies on January 26, 2026. The candies contain undeclared allergens including milk, soy, and peanuts. Consumers should stop using the product immediately and seek a refund or replacement.

Beacon Promotions
Undeclared allergens
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HIGHFDA DRUG

Asteria Health Recalls Testosterone Pellets Due to Metal Contamination

Asteria Health recalled 1,464 testosterone pellets on January 26, 2026, due to potential metal particulate contamination. The recall affects products distributed nationwide. Consumers must stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 5 M12 Over Safety Risk

Philips Medical Systems recalled 326 Azurion 5 M12 systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a risk to patients and healthcare providers. Immediate cessation of use is advised.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 7 B20 System Over Movement Risk

Philips Medical Systems recalled 1,503 Azurion 7 B20 systems on January 26, 2026. The devices may move unexpectedly when the Reset Geometry button is pressed, posing a risk of injury. Healthcare providers must stop using the device and follow recall instructions immediately.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 5 M20 Table Over Movement Hazard

Philips Medical Systems Nederland B.V. recalled 922 Azurion 5 M20 systems on January 26, 2026, due to a defect that causes unexpected table movement. This hazard can occur even with an active table lock when the Reset Geometry button is pressed. The recall includes 101 units in the U.S. and 821 units distributed worldwide.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 3 M12 Due to Hazard

Philips Medical Systems recalled 291 Azurion 3 M12 systems on January 26, 2026, due to a risk of unexpected table movement. This may occur when the Reset Geometry button is pressed, even if a table lock is active. The recall affects 27 units in the U.S. and 264 units internationally.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 7 B12 Table Due to Safety Risk

Philips Medical Systems Netherlands B.V. recalled 655 Azurion 7 B12 systems on January 26, 2026. The recall affects models 722067, 722225, and 722235 due to unexpected table movement when the Reset Geometry button is pressed. This poses a high risk of injury to patients and healthcare providers.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DEVICE

Philips Medical Systems Recalls Azurion 7 M12 Due to Hazardous Movement

Philips Medical Systems recalled 1,979 Azurion 7 M12 Systems on January 26, 2026. The table may move unexpectedly when the Reset Geometry button is pressed, posing a high risk of injury. Healthcare providers and patients should stop using the devices immediately.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Under certain
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HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 50,990 Estradiol pellets on January 26, 2026, due to potential metal particulate matter contamination. The recall affects products distributed nationwide in the USA. Consumers should stop using the pellets immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Due to Metal Contamination

Asteria Health recalled 133 estradiol pellets on January 26, 2026, after detecting potential metal particulate matter. The recall, classified as Class II, affects pellets with lot number 253000126 and an expiration date of June 9, 2026. Consumers must stop using the product immediately and contact their healthcare provider for guidance.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Over Metal Contamination

Asteria Health recalled 1,699 sterile estradiol pellets on January 26, 2026, due to potential metal particulate contamination. Consumers should stop using the product immediately and contact their healthcare provider for advice. The recall affects pellets distributed nationwide in the USA.

F.H. INVESTMENTS, Inc.
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HIGHFDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination

Asteria Health recalled 60,868 testosterone pellets on January 26, 2026, due to contamination risks. The recall affects specific lots of the product that may contain metal particulate matter. Consumers must stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Over Metal Contamination Risk

Asteria Health recalled 14,848 estradiol pellets on January 26, 2026, due to potential metal particulate contamination. Consumers and healthcare providers must stop using the product immediately. The recall is classified as Class II, indicating a high hazard level.

F.H. INVESTMENTS, Inc.
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HIGHFDA DRUG

Asteria Health Recalls Estradiol Pellets Due to Metal Particles

Asteria Health recalled 715 units of Estradiol, 37.5 mg pellets on January 26, 2026. The recall follows the potential presence of metal particulate matter in the product. Consumers should stop using the pellets immediately and contact their healthcare provider for further guidance.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contaminants

Asteria Health recalled 4,599 testosterone pellets on January 26, 2026. The recall follows concerns over potential metal particulate matter contamination. Consumers should stop using the product immediately and seek guidance from healthcare providers.

F.H. INVESTMENTS, Inc.
Presence of
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HIGHFDA DRUG

Asteria Health Recalls Testosterone Pellets Over Metal Contamination Risk

Asteria Health recalled 1,015 testosterone pellets on January 26, 2026 due to potential metal particulate contamination. The recall affects products distributed nationwide in the United States. Consumers must stop using the pellets immediately and contact their healthcare provider for guidance.

F.H. INVESTMENTS, Inc.
Presence of
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