RecallRadar

FDA Drug recall D-0008-2017

PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-4741-25

On 2016-10-12 the FDA classified a Class II recall of PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-4741-25 by West Ward Pharmaceutical, citing failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0008-2017
ClassificationClass II
Statusterminated
Initiated2016-10-03
Published2016-10-12
Last updated2026-09-13 11:51 UTC
CompanyWest Ward Pharmaceutical
DistributionUS

Product

PredniSONE Tablets USP, 1 mg, 100-count bottles, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC 0054-4741-25.

Reason

Failed Tablet/Capsule Specifications: Discovery of an underweight tablet.

Identifiers

ndc0054-4741-25
ndc0054-4741-31
ndc0054-4742-25
ndc0054-4728-25
ndc0054-4728-31
ndc0054-0017-25
ndc0054-0017-29
ndc0054-0017-20
ndc0054-0018-25
ndc0054-0018-29
ndc0054-0018-20
ndc0054-0019-20
ndc0054-0019-25
ndc0054-3722-63
ndc0054-3722-50
ndc0054-3721-44
ndc0054-8739-25
ndc0054-8740-25
ndc0054-8724-25
code_infoLot # 660621A, Exp 01/31/18

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-0008-2017%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.