FDAFDA · Food and drugs·Recall number D-0842-2020
Caduet (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.
Published February 19, 2020 · Recall initiated: February 5, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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
Voluntary: Firm initiated · Letter
Recall details
- Brand
- CADUET
- Manufacturer
- Pfizer Inc.
- Distributor
- Nationwide in the USA.
- UPC
- 0300692150305
- Lot
- Lot #: CY0963, Exp 07/2022
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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