These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
- High-risk recalls
- 4,262
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)
Siemens MAGNETOM Verio Dot Upgrade MRI Recalled Over Ice Blockage Risk (46 Units) 2025
Siemens MRI Recall: 18 MAGNETOM Skyra Fit BioMatrix Systems Recalled Over Helium Vent Blockage Risk
Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk
Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.
Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System
Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)
Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak
Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System
Green Lumber Natural Fuel For Men Capsules Recalled for Tadalafil Contamination
Marketed without an Approved NDA/ANDA: FDA analysis found this product to contain tadalafil
Middlefield Original Cheese Cooperative Smoked Cheddar Recalled for Listeria Risk in 2025
Potential contamination with Listeria monocytogenes
Chlorpromazine Hydrochloride Tablets Recalled Nationwide for Foreign Substance in Packaging Lot 1022
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Zydus Lifesciences Succinylcholine Chloride Injection Recall Active for Unknown Impurity Degradation
Failed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.
Unichem Pharmaceuticals USA Cyclobenzaprine Recall for Label Mix-Up Affects 230 Bottles (2025)
Labeling: Label Mix Up; Bottles of Meloxicam USP, 7.5mg, 90-count tablets (yellow in color), were labeled as Cyclobenzaprine Hydrochloride Tablets USP, 10 mg 90-count tablets (blue in color).
Chlorpromazine Hydrochloride 25 mg Tablets Recalled Nationwide Over Foreign Substance in Packaging
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride Tablets Recalled Over Foreign Substance Found in Packaging Coil (High-R
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging at the manufacturing site, was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Sunrise Creamery Dilly Pickle Monterey Jack Cheese Recalled Over Listeria Risk (2025) by Middlefield
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative Swiss Cheese Recall for Listeria Contamination (2025)
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative Recalls 5 lb Shredded Mozzarella Over Listeria Risk (2025)
Potential contamination with Listeria monocytogenes
Middlefield Original Cheese Cooperative Pepper Jack Cheese Recalled Over Listeria Risk in 364 Cases
Potential contamination with Listeria monocytogenes