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Class II · ModerateActive recall

Atorvastatin Calcium

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot # F117192201, Exp. Date 4/30/2023
Where it was soldNationwide with the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

CGMP Deviations

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byNorthwind Health Company, LLC
Brand nameATORVASTATIN CALCIUM
Generic nameATORVASTATIN CALCIUM
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Distributed by / forNorthwind Pharmaceuticals LLC
NDC51655-946-52
Show the full FDA record
Full product labelAtorvastatin Calcium Tablets, USP, 10 mg, 30-count bottles, Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203. NDC 51655-946-52
Recalling firmNorthwind Pharmaceuticals LLC
DistributionNationwide with the United States
Quantity99 bottles
Recall initiated2023-03-16
Report date2023-05-03
Recall completed—
Recall numberD-0548-2023
ClassificationClass II
FDA statusOngoing
Origin on fileIndianapolis IN United States

Related

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Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.