RecallRadar

FDA Drug recall D-0842-2020

Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/10 mg*, 30-count bottle, Rx only, Distributed by: Pfizer Labs, Division of…

On 2020-02-19 the FDA classified a Class II recall of Caduet (amlodipine besylate/atorvastatin calcium) Tablets, 10 mg/10 mg*, 30-count bottle, Rx only, Distributed by: Pfizer Labs, Division of… by Pfizer, citing 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….

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0842-2020
ClassificationClass II
Statusterminated
Initiated2020-02-05
Published2020-02-19
Last updated2026-09-13 11:52 UTC
CompanyPfizer
DistributionUS

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

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.

Identifiers

ndc0069-2150-30
ndc0069-2170-30
ndc0069-2190-30
ndc0069-2260-30
ndc0069-2160-30
ndc0069-2180-30
ndc0069-2250-30
ndc0069-2270-30
ndc0069-6180-30
ndc0069-6323-30
ndc0069-6565-30
ndc0069-6747-30
ndc0069-7810-30
ndc0069-7232-30
ndc0069-7654-30
ndc0069-7476-30
code_infoLot #: CY0963, Exp 07/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0842-2020%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.