RecallRadar

FDA Drug recall D-0091-2018

Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217

On 2017-11-29 the FDA classified a Class II recall of Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217 by Amerisource Health Services, citing presence of Foreign Tablets/Capsules.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0091-2018
ClassificationClass II
Statusterminated
Initiated2017-10-24
Published2017-11-29
Last updated2026-09-13 11:51 UTC
CompanyAmerisource Health Services
DistributionUS

Product

Paroxetine Tablets, USP, 30mg, 100 tablets (10 x 10) , Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Columbus, Ohio 43217, NDC 68084-046-01

Reason

Presence of Foreign Tablets/Capsules.

Identifiers

ndc68084-044-11
ndc68084-044-01
ndc68084-044-65
ndc68084-045-11
ndc68084-045-01
ndc68084-046-11
ndc68084-046-01
ndc68084-047-11
ndc68084-047-01
code_infoLot 172291

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0091-2018%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.