RecallRadar

FDA Drug recall D-882-2013

Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Col…

On 2013-08-21 the FDA classified a Class III recall of Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Col… by Boehringer Ingelheim Roxane, citing labeling: Missing Label; missing label on blister card.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-882-2013
ClassificationClass III
Statusterminated
Initiated2013-06-14
Published2013-08-21
Last updated2026-09-13 11:51 UTC
CompanyBoehringer Ingelheim Roxane
DistributionUS

Product

Prednisone Tablet USP, 20 mg tablets, packaged in blisters of ten (10) tablets per blister card, ten blister cards per carton, Roxanne, Columbus, OH --- NDC 0054-0018-20

Reason

Labeling: Missing Label; missing label on blister card

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_infoThe affected product consists of lot #261739A, expiration date OCT 2014.

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-882-2013%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.