Drug recall D-0842-2020
Product
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.
Reason for recall
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.
Lots and codes
Lot #: CY0963, Exp 07/2022
Recall details
- Recalling firm
- Pfizer Inc., New York, NY
- Quantity
- 128 bottles
- Distribution
- Nationwide in the USA.
- Type
- Voluntary: Firm initiated
- Recall initiated
- February 5, 2020
- Terminated
- March 8, 2021
Related products
- Caduet – drug information
- NDC 0069-7232 Caduet · Amlodipine Besylate 10 mg/1; Atorvastatin Calcium… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-6747 Caduet · Amlodipine Besylate 5 mg/1; Atorvastatin Calcium Trihydrate… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-7654 Caduet · Amlodipine Besylate 10 mg/1; Atorvastatin Calcium… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-6323 Caduet · Amlodipine Besylate 5 mg/1; Atorvastatin Calcium Trihydrate… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-7810 Caduet · Amlodipine Besylate 10 mg/1; Atorvastatin Calcium… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-6180 Caduet · Amlodipine Besylate 5 mg/1; Atorvastatin Calcium Trihydrate… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-6565 Caduet · Amlodipine Besylate 5 mg/1; Atorvastatin Calcium Trihydrate… · Pfizer Laboratories Div Pfizer Inc
- NDC 0069-7476 Caduet · Amlodipine Besylate 10 mg/1; Atorvastatin Calcium… · Pfizer Laboratories Div Pfizer Inc