Drug recalls, by class and condition
Every Class I, II, and III recall from the FDA Enforcement Report database, in chronological order. Class I is the most serious.
In the last 30 days, FDA issued 1 Class I recall (most serious), 16 Class II, and 8 Class III affecting the medications we cover.
Sourced from FDA Enforcement Reports. Verify on FDA →
October 22, 20252 recalls
October 15, 20251 recall
September 24, 20251 recall
September 17, 20252 recalls
September 3, 20251 recall
August 27, 20251 recall
August 20, 20252 recalls
Recalls by condition
- Blood pressure medication recalls36 activeLisinopril, Losartan, Amlodipine, Valsartan
- Cholesterol medication recalls10 activeAtorvastatin, Rosuvastatin, Simvastatin
- Diabetes drug recalls20 activeMetformin, Insulin Glargine, Sitagliptin
- ADHD medication recalls0 activeAmphetamine, Methylphenidate, Atomoxetine
How FDA classifies recalls
Class I: The drug may cause serious health consequences or death. Examples include the wrong drug in a bottle, a drug contaminated with bacteria, or a life-threatening allergen not declared on the label.
Class II: The drug may cause temporary or medically reversible adverse health consequences, or the probability of serious consequences is remote. Examples include a dissolution failure, a labeling error that affects dosing, or a nitrosamine impurity above the daily intake limit.
Class III: Use of the drug is unlikely to cause adverse health consequences, but the product violates FDA regulations. Examples include an incorrect tablet count per bottle, minor labeling issues, or packaging defects.
Definitions sourced from FDA Recall Classifications →