stop use immediately Recalls

1,862 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical Recalls MRI Machine Over Helium Leak Risk

Siemens Medical Solutions USA recalled 182 MRI machines on August 28, 2025, due to a risk of helium leaks. An ice blockage in the magnet venting system could cause pressure build-up, leading to a potential rupture. Users must stop using the device and follow recall instructions immediately.

Siemens Medical Solutions USA
There is
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MRI System Recalled Due to Helium Leak Risk

Siemens Medical Solutions USA recalled 69 units of the MAGNETOM Verio MRI system on August 28, 2025. Ice blockage in the magnet venting system could lead to a helium leak, posing serious risks. Healthcare providers must stop using the device immediately and follow recall instructions.

Siemens Medical Solutions USA
There is
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Co-op Recalls Organic Gouda Over Listeria Risk

Middlefield Original Cheese Co-op recalled 364 cases of Organic Gouda Cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes, which can cause serious illness. Consumers should not eat the cheese and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Middlefield Cheese Coop Recalls Cheddar Cheese for Listeria Risk

Middlefield Original Cheese Cooperative recalled 364 cases of cheddar cheese on August 27, 2025. The products may contain Listeria monocytogenes, a harmful bacteria. Consumers should avoid eating the cheese and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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Food & Beverages
HIGH
FDA FOOD

Sunrise Creamery Cheese Recalled Due to Listeria Risk

Sunrise Creamery recalled 364 cases of Dilly Pickle Monterey Jack Cheese on August 27, 2025. The product may contain Listeria monocytogenes, posing a serious health risk. Consumers should avoid eating this cheese and seek refunds immediately.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

American Health Packaging Recalls Chlorpromazine Tablets Over Contamination Risk

American Health Packaging recalled 1,757 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall stems from the detection of a microorganism in packaging materials, though no contamination was found on the tablets themselves. Consumers should stop using the product immediately and contact healthcare providers for guidance.

Chlorpromazine Hydrochloride
Presence of
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Food & Beverages
HIGH
FDA FOOD

Middlefield Cheese Co-op Issues Recall for Smoked Cheddar Due to Listeria Risk

Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar on August 27, 2025. The cheese may be contaminated with Listeria monocytogenes, posing a high health risk. Consumers in Ohio, Pennsylvania, Wisconsin, and Texas should not consume the product.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride Tablets Recalled Due to Contamination Risk

American Health Packaging recalled 2,708 cartons of Chlorpromazine Hydrochloride Tablets on August 27, 2025. The recall follows the detection of a micro-organism in product packaging, though no contamination was found on the tablets themselves.

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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Food & Beverages
HIGH
FDA FOOD

Middlefield Cheese Recalled Due to Listeria Contamination Risk

Middlefield Original Cheese Cooperative recalled 364 cases of Pepper Jack Cheese on August 27, 2025. The recall follows potential contamination with Listeria monocytogenes. Consumers should not eat the product and seek refunds or replacements.

Middlefield Original Cheese Cooperative
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Unichem Pharmaceuticals Recalls Cyclobenzaprine Tablets Due to Labeling Error

Unichem Pharmaceuticals recalled 230 bottles of Cyclobenzaprine Hydrochloride Tablets on August 27, 2025. The recall stems from a labeling mix-up with Meloxicam tablets, which could lead to serious health risks. Consumers should stop using the product immediately and contact their healthcare provider.

CYCLOBENZAPRINE HYDROCHLORIDE
Labeling: Label
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Health & Personal Care
HIGH
FDA DRUG

Zydus Pharmaceuticals Recalls Succinylcholine Chloride Injection Due to Hazards

Zydus Pharmaceuticals recalled 270,125 vials of Succinylcholine Chloride Injection on August 27, 2025. The recall follows failed impurity tests indicating unknown degradation issues. Consumers and healthcare providers must stop using the product immediately and seek guidance.

Succinylcholine Chloride
Failed Impurities/Degradation
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Health & Personal Care
HIGH
FDA DRUG

Neuroquell Recall Issued Over cGMP Violations

Claire Ellen Products recalled 72 containers of Neuroquell and Neuroquell Plus on August 27, 2025. The recall follows violations of current Good Manufacturing Practices (cGMP). Consumers must stop using the products immediately and consult healthcare providers for guidance.

Claire Ellen Products
cGMP violations
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Health & Personal Care
HIGH
FDA DEVICE

Vision RT Recalls AlignRT InBore System Over Laser Omission Hazard

Vision RT recalled 56 AlignRT InBore systems on August 27, 2025, due to missing safety information in the Instructions for Use. The omission pertains to the identification and characteristics of the system's Class 1 lasers as required by federal regulations. Users must stop using the device immediately and follow manufacturer instructions.

Vision RT
Vision RT
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Medical Issues Recall for Sodium Chloride Irrigation Solution

B. Braun Medical Inc. recalled 16,228 bags of Sodium Chloride Irrigation Solution on August 26, 2025. The recall stems from a lack of assurance of sterility, posing a high risk of contamination. Consumers and healthcare providers should stop using the product immediately and seek guidance from B. Braun or their healthcare provider.

B. Braun Medical Inc.
Lack of
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Recalls Gummies Due to Peanut Protein Risk

Extract Labs recalled 2,180 bottles of sugar-free mixed berry gummies on August 26, 2025. The recall stems from potential peanut protein cross-contact, posing a risk to consumers with allergies. The gummies contain 10mg of CBD and 10mg of D9 THC per serving.

Extract Labs
Potential peanut
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Medical Recalls Sterile Water for Injection Due to Sterility Risk

B. Braun Medical Inc. recalled 26,316 bags of Sterile Water for Injection on August 26, 2025. The recall affects the 3000 mL product due to potential fluid leakage from a misaligned port. Consumers should stop using the product immediately and seek guidance from healthcare providers.

B. Braun Medical Inc.
Lack of
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Recalls Mai Tai Gummies Over Peanut Protein Risk

Extract Labs recalled 19,750 gummies on August 26, 2025, due to potential peanut protein cross-contact. The products, which contain 20mg of CBD and 20mg of D9 THC per gummy, lack proper labeling. Consumers should not consume these gummies and should contact the company for refunds or replacements.

Extract Labs
Potential peanut
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Recalls Elderberry Gummies Over Peanut Protein Risk

Extract Labs recalled 19,720 Elderberry gummies on August 26, 2025 due to potential peanut protein cross-contact. The gummies, containing 20mg CBD and 20mg D9 THC each, were shipped unlabeled in bulk packaging. Consumers should not consume these products and seek refunds or replacements.

Extract Labs
Potential peanut
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