Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues
Granules Pharmaceuticals
Failed Impurities/Degradation
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Recall: 11,928 Bottles of Dextroamphetamine Mixed Salts Suspended for Impur
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Extractor Pro RX Balloon Catheter Recalled Over Labeling Error (2025)
The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.
Boston Scientific
The product
Health & Personal Care
HIGH
FDA DRUG
Granules Pharmaceuticals Dextroamphetamine Mixed Salts ER Capsules Recall 11,909 Bottles (2025)
Granules Pharmaceuticals
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical Solutions USA MAGNETOM Prisma MRI Recalled for Ice Blockage Risk in 39 Units (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Howmedica Osteonics Recalls 55 EXETER V40 Surgical Stems Due to Product Mix Risk
a potential product mix where the package labeled as Catalog Number 0580-1-442, lot A00976, may contain Catalog Number 0580-1-352, lot G8754849, and vice versa. Patient labels may also be impacted.
Howmedica Osteonics
a potential
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio Dot Upgrade MRI Recalled Over Ice Blockage Risk (46 Units) 2025
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens Biograph mMR PET-MRI Recall 2025 for Ice Blockage Risk in Venting System (23 Units)
Siemens
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio Dot MRI Recall 30 Units Over Ice Blockage Risk (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
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 Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Cima.X MRI Recall: 9 Units Worldwide (2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Skyra fit MRI Recalled for Ice Blockage Risk in 30 Units (2025)
Siemens Medical Solutions USA
There is
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
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical Solutions USA BIOGRAPH One MRI System Recalled for Helium Leak Risk (1 Unit, 2025)
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DEVICE
Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak
Siemens Medical Solutions USA
There is
Health & Personal Care
HIGH
FDA DRUG
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
Green Lumber Holdings
Marketed without
Health & Personal Care
HIGH
FDA DRUG
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).
CYCLOBENZAPRINE HYDROCHLORIDE
Labeling: Label
Health & Personal Care
HIGH
FDA DRUG
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.
CHLORPROMAZINE HYDROCHLORIDE
Presence of
Health & Personal Care
HIGH
FDA DRUG
Claire Ellen Products Neuroquell & Neuroquell Plus Recall: 72 Containers in 2025
Claire Ellen Products
cGMP violations
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