Caduet — Class II drug recall D-0842-2020
Terminated recall by Pfizer Inc., reported 2020-02-19, distributed nationwide. Defective Container: products potentially could have been packaged in defective bottles, with a notched rim, t
| Recall number | D-0842-2020 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Pfizer Inc., New York, NY, United States |
| Recall initiated | 2020-02-05 |
| Classified | 2020-02-13 |
| Reported by FDA | 2020-02-19 |
| Terminated | 2021-03-08 |
| Distributed | Nationwide (US) |
| Quantity | 128 bottles |
| Reason classes | packaging |
| NDC | 00069-2150, 00069-2150-30, 00069-2160, 00069-2160-30, 00069-2170, 00069-2170-30, 00069-2180, 00069-2180-30, 00069-2190, 00069-2190-30, 00069-2250, 00069-2250-30, 00069-2260, 00069-2260-30, 00069-2270, 00069-2270-30, 00069-6180, 00069-6180-30, 00069-6323, 00069-6323-30, 00069-6565, 00069-6565-30, 00069-6747, 00069-6747-30, 00069-7232 and 7 more |
| Lot numbers | CY0963 |
| Expiration dates | 2022-07 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0842-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.