cpsc regulated Recalls

2,056 recalls tagged with “cpsc regulated”.

Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Verio Dot MRI Recall 30 Units Over Ice Blockage Risk (2025)

Siemens Medical Solutions USA recalled 30 MAGNETOM Verio Dot MRI systems sold worldwide through hospitals and medical facilities. The ice blockage in the magnet venting system could trap helium during a quench, causing pressure buildup and a potential helium leak into the scanning room. Facilities should stop using the devices immediately and follow the manufacturer’s recall instructions.

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

Siemens Biograph mMR PET-MRI Recall 2025 for Ice Blockage Risk in Venting System (23 Units)

Siemens Medical Solutions USA recalled 23 Biograph mMR PET-MRI systems worldwide after detecting an ice blockage in the magnet venting system. In a magnet quench, helium gas may not escape through vent paths, risking rupture of the helium containment and a leak into the scanning room. Hospitals and providers must stop using the device immediately and follow the manufacturer’s recall instructions.

Siemens
There is
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)

Siemens Medical Solutions USA recalls MAGNETOM Spectra MRI with Model Number 10655588 after possible ice blockage in the magnet venting system could cause a helium leak during a quench. The recall covers worldwide distribution including the United States. Patients should stop using the device and follow manufacturer instructions for recall procedures.

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

Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System

Siemens Medical Solutions USA recalls 69 MAGNETOM Verio MRIs worldwide after an ice blockage could trap helium gas during a quench. A rupture of the helium containment system may leak helium into the scanning room. The recall affects models with number 10276755 and serials including 40649 and others. Patients and providers should stop using the device and follow manufacturer instructions.

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

Siemens MRI Recall: 18 MAGNETOM Skyra Fit BioMatrix Systems Recalled Over Helium Vent Blockage Risk

Siemens Medical Solutions USA recalls 18 MAGNETOM Skyra Fit BioMatrix MRI systems worldwide due to ice blockage in the magnet venting system that could trap helium gas during a quench. The risk is a ruptured helium containment and a potential helium leak into the scanning room. Hospitals and clinicians should stop using the affected devices and await manufacturer instructions.

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

Middlefield Original Cheese Cooperative Recalls 7,455 lbs Shredded Mozzarella/Provolone (5-lb Bags)

Middlefield Original Cheese Cooperative recalled 364.125 cases of shredded Mozzarella/Provolone cheese sold in Ohio, Pennsylvania, Wisconsin, and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who purchased this product should not consume it and should contact the cooperative for refund or replacement information.

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

Middlefield Original Cheese Co-op Recalling 7,455 lbs of Cheese Loaves Over Listeria Contamination (

Middlefield Original Cheese Co-op is recalling 7,455 pounds of Monterey Jack and Provolone cheese loaves. The products were distributed to Ohio, Pennsylvania, Wisconsin and Texas. The recall is due to potential contamination with Listeria monocytogenes. Consumers who bought these loaves should not consume them and should contact the cooperative for refund or replacement.

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

Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025

Middlefield Original Cheese Cooperative recalled 364.125 cases of Smoked Cheddar loaves sold through multiple retailers in Ohio, Pennsylvania, Wisconsin and Texas after a Listeria monocytogenes concern. The recall is Class I and carries a high hazard. Consumers who bought this product should not consume it and should contact the cooperative for refund or replacement information.

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

Claire Ellen Products Neuroquell & Neuroquell Plus Recall: 72 Containers in 2025

Claire Ellen Products recalled 72 containers of Neuroquell and Neuroquell Plus after cGMP violations were identified. The recall covers 0.22 fl oz bottles distributed online. Consumers should stop using the product immediately and contact Atlantic Management Resources Ltd. via email for guidance.

Claire Ellen Products
cGMP violations
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Food & Beverages
HIGH
FDA FOOD

Middlefield Organic Gouda Cheese Recall: 364 Cases Over Listeria Contamination (2025)

Middlefield Original Cheese Cooperative is recalling 364 cases of Organic Gouda Cheese, 8 oz, packaged 12 per case and distributed in Ohio, Pennsylvania, Wisconsin and Texas, after potential contamination with Listeria monocytogenes. The product poses a high risk of serious illness if consumed. Consumers should not eat the cheese and should contact the cooperative for a refund or replacement.

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

Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled Over Listeria Risk in 364 Cases

Middlefield Original Cheese Cooperative Pepper Jack Cheese is recalled across Ohio, Pennsylvania, Wisconsin and Texas. The recall covers 364.125 cases, about 7,455 pounds, due to potential contamination with Listeria monocytogenes. Consumers should not consume the product and should contact Middlefield Original Cheese Cooperative for refund or replacement information.

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

Chlorpromazine Hydrochloride Tablets Recalled Nationwide for Foreign Substance in Packaging Lot 1022

A high-severity recall covers chlorpromazine hydrochloride tablets distributed nationwide by American Health Packaging. A foreign substance linked to a polyester coil packaging component was detected at the manufacturing site. No tablets were contaminated. Stop using the product and contact the distributor for guidance.

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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Food & Beverages
HIGH
FDA FOOD

Middlefield Original Cheese Cooperative Recalls 5 lb Shredded Mozzarella Over Listeria Risk (2025)

Middlefield Original Cheese Cooperative recalled 364.125 cases of 5 lb shredded mozzarella cheese sold to retailers in Ohio, Pennsylvania, Wisconsin and Texas. The product could be contaminated with Listeria monocytogenes. Consumers should not consume it and should contact the cooperative for refund or replacement.

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

Sunrise Creamery Dilly Pickle Monterey Jack Cheese Recalled Over Listeria Risk (2025) by Middlefield

Sunrise Creamery Monterey Jack Cheese with Dill Pickles is recalled by Middlefield Original Cheese Cooperative after FDA findings indicate potential Listeria monocytogenes contamination. The recall covers two SKUs in 6 oz and 1.25 lb sizes, distributed to Ohio, Pennsylvania, Wisconsin and Texas. Consumers should discard affected cheese and contact the cooperative for refund or replacement.

Sunrise Creamery
Potential contamination
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride Tablets Recalled Over Foreign Substance Found in Packaging Coil (High-R

Chlorpromazine Hydrochloride tablets distributed nationwide by American Health Packaging are recalled after a polyester coil used in packaging showed presence of a micro-organism in a specific lot. No tablets were contaminated. Consumers and healthcare providers should stop using this product immediately and contact Amerisource Health Services LLC for guidance.

Chlorpromazine Hydrochloride
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Chlorpromazine Hydrochloride 25 mg Tablets Recalled Nationwide Over Foreign Substance in Packaging

A recall of chlorpromazine hydrochloride tablets is active nationwide in the United States. A specific lot of packaging material to coils used in manufacturing contained a foreign substance with a microorganism detected. Tablets themselves tested negative for microorganisms. Consumers and healthcare providers should stop using the product immediately and contact Amerisource Health Services LLC or

CHLORPROMAZINE HYDROCHLORIDE
Presence of
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Food & Beverages
HIGH
FDA FOOD

Extract Labs Blue Razz 20mg CBD/THC Gummies Recall 2025 for Peanut Cross-Contact — 19,810 Units

Extract Labs recalled 19,810 Blue Razz 20mg CBD/THC gummies distributed across the United States and Australia, as well as Germany, the United Kingdom, Malaysia and New Zealand. The unlabelled bulk product was shipped in poly gusset bags inside brown boxes. Consumers who may have peanut allergies should not consume the product; contact Extract Labs for a refund or replacement via email.

Extract Labs
Potential peanut
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Vehicles & Parts
HIGH
NHTSA

Hyundai Recalls 2025-2026 Santa Fe and Tucson for Engine Fastener Issue

Hyundai Motor America is recalling certain 2025-2026 Tucson and Santa Fe vehicles. The connecting rod bolts may have been improperly tightened, which can cause a loss of drive power and engine damage, potentially resulting in an oil leak. Owner notification letters are expected to be mailed October 24, 2025, and dealers will replace the engine free of charge.

Hyundai
A loss
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Health & Personal Care
HIGH
FDA DRUG

B. Braun Medical 3000 mL Saline Irrigation Bags Recalled for Sterility Concerns

B. Braun Medical Inc. recalled 16,228 3000 mL saline irrigation bags nationwide in the United States. The recall cites lack of assurance of sterility due to port misalignment, creating a potential for fluid leakage. Healthcare providers and patients should stop using the product immediately and contact the company for guidance.

B. Braun Medical Inc.
Lack of
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Tag Statistics

Total Recalls
2,056

Related Tags

immediate actionreturn for refundfda regulatedelectronicbattery poweredreplacement availableworkplacestop use immediatelyrepair availablefire hazardchemical hazardelectrical hazard