electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

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 Verio Dot Upgrade MRI Recalled Over Ice Blockage Risk (46 Units) 2025

Siemens Medical Solutions USA recalled 46 MAGNETOM Verio Dot Upgrade MRI systems sold to hospitals worldwide after an ice blockage could prevent venting during a quench. The blockage could cause pressure to build in the helium containment system, potentially rupturing it and releasing helium into the scanning room. Hospitals and providers should stop using the device immediately and follow Siemens

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

Siemens MAGNETOM Cima.X MRI Recall: 9 Units Worldwide (2025)

Siemens Medical Solutions USA recalled 9 MAGNETOM Cima.X MRI systems worldwide. A potential ice blockage in the magnet venting system could prevent helium from escaping during a quench, risking rupture and a helium leak into the scanning room. Hospitals and healthcare providers should stop using the devices and follow the manufacturer’s recall 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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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System

Siemens Medical Solutions USA issued a global recall for the MAGNETOM Connectom.X MRI system, Model 11371480. One unit is affected. A potential ice blockage in the magnet venting system could cause a helium leak during a quench. Users should stop using the device and await manufacturer instructions.

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

Howmedica Osteonics Recalls 55 EXETER V40 Surgical Stems Due to Product Mix Risk

Howmedica Osteonics recalled 55 units of EXETER V40 surgical stems distributed in the United Kingdom due to a risk of product mix. Patients may receive the incorrect product, potentially leading to surgical complications. Patients and healthcare providers must stop using the device and follow the manufacturer’s instructions.

Howmedica Osteonics
a potential
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak

Siemens Medical recalled 27 MAGNETOM Vida Fit MRI systems after a potential helium containment rupture was identified. Ice blockage in the magnet venting system may prevent helium from escaping, leading to a dangerous pressure build-up. Patients and healthcare providers must stop using the device immediately and follow the manufacturer's instructions.

Siemens Medical Solutions USA
There is
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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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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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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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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

Zydus Lifesciences Succinylcholine Chloride Injection Recall Active for Unknown Impurity Degradation

Zydus Lifesciences recall remains active for 270,125 vials distributed across MS, OH, LA and Puerto Rico. The FDA notice cites failed impurities and degradation specifications as the reason. Immediate discontinuation is advised for healthcare providers and patients with ongoing prescriptions. Contact Zydus Pharmaceuticals USA Inc for guidance.

Zydus Lifesciences
Failed Impurities/Degradation
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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 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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Food & Beverages
HIGH
FDA FOOD

Country Eggs Shell Egg Recall Affects 81,542 Dozen Across CA and NV

Country Eggs LLC recalled 81,542 dozen shell eggs distributed to 11 consignees in California and Nevada due to potential salmonella contamination. The recall covers Nagatoshi, Nijiya, Mizuho, and Sunshine yolk varieties sold in large AA Brown egg cartons. Consumers should not eat these eggs and should seek refund or replacement.

Country Eggs
Shell egg
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Health & Personal Care
HIGH
FDA DEVICE

CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle

CooperVision recalled one lot of Voyant 1-Day Premium Toric contact lenses sold nationwide in the United States after an invalid sterilization cycle was detected. The recall affects 90 units distributed in Florida, Kentucky, North Carolina and Wisconsin. Patients should stop using the lenses immediately and contact their eye care professional for guidance.

CooperVision
One lot
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Vehicles & Parts
HIGH
NHTSA

Ford Recalls 2025 Explorer and Aviator for Trailer Tail Light Failure (25C42)

Ford recalls 2025 Explorer and Aviator vehicles sold through Ford dealers due to a faulty body control module that can prevent trailer tail lights from illuminating. The defect may reduce visibility for other drivers when towing a trailer. Interim letters alert owners starting Oct 13, 2025, with a final remedy anticipated in April 2026. Ford will perform the repairs at no charge and provide the an

Ford
Trailer tail
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Tag Statistics

Total Recalls
1,120

Related Tags

fire hazardchemical hazardstop use immediatelyimmediate actionreplacement availablecpsc regulatedfda regulatedholiday productpet relatedkitchenbathroominfant product