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Class II · ModerateRecall completed

Caduet

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

Does this affect you?
Check your lot numberLot #: CY0963, Exp 07/2022
Where it was soldNationwide in the USA.
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

Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, that could cause inadequate foil sealing resulting in lack of moisture protection.

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 byMade in Germany foreign manufacturer
Brand nameCADUET
Generic nameAMLODIPINE AND ATORVASTATIN
Active ingredient(s)AMLODIPINE BESYLATE, ATORVASTATIN CALCIUM TRIHYDRATE
Distributed by / forPfizer Labs, Division of Pfizer Inc. NY, NY 10017
NDC0069-2160-30
Show the full FDA record
Full product labelCaduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/10 mg*, 30-count bottle, Rx only, Distributed by: Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Germany, NDC 0069-2160-30.
Recalling firmPfizer Inc.
DistributionNationwide in the USA.
Quantity128 bottles
Recall initiated2020-02-05
Report date2020-02-19
Recall completed2021-03-08
Recall numberD-0842-2020
ClassificationClass II
FDA statusTerminated
Origin on fileNew York NY United States

Related

Recent drug recallsCheck another medication

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.