RecallRadar

FDA Drug recall D-0699-2021

Chantix (varenicline) tablets, 0.5mg*, 56 Tablets, Rx Only, Distributed by Pfizer Labs, Division of Pfizer Inc., NY, NY 10017, Made in Irel…

On 2021-08-11 the FDA classified a Class II recall of Chantix (varenicline) tablets, 0.5mg*, 56 Tablets, Rx Only, Distributed by Pfizer Labs, Division of Pfizer Inc., NY, NY 10017, Made in Irel… by Pfizer, citing CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s acceptable interim acceptable intake limit.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0699-2021
ClassificationClass II
Statusongoing
Initiated2021-06-09
Published2021-08-11
Last updated2026-09-13 11:52 UTC
CompanyPfizer
DistributionUS

Product

Chantix (varenicline) tablets, 0.5mg*, 56 Tablets, Rx Only, Distributed by Pfizer Labs, Division of Pfizer Inc., NY, NY 10017, Made in Ireland. NDC 0069-0468-56

Reason

CGMP Deviations: Presence of the N-nitroso-varenicline impurity above FDA s acceptable interim acceptable intake limit

Identifiers

ndc0069-0468-56
ndc0069-0469-56
ndc0069-0469-28
ndc0069-0471-03
ndc0069-0471-28
code_infoLots 00019213, Exp 31 Jan 2022 & EC6994, Exp May 31, 2023

Status history

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

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0699-2021%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.