Data Foundry

Drug recalls 2013

Prednisone Tablet USP — Class III drug recall D-882-2013

Terminated recall by Boehringer Ingelheim Roxane Inc, reported 2013-08-21, distributed nationwide. Labeling: Missing Label; missing label on blister card

Recall numberD-882-2013
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBoehringer Ingelheim Roxane Inc, Columbus, OH, United States
Recall initiated2013-06-14
Classified2013-08-12
Reported by FDA2013-08-21
Terminated2014-06-23
DistributedNationwide (US)
Quantity14,619 cartons
Reason classeslabeling
NDC00054-0017, 00054-0017-20, 00054-0017-25, 00054-0017-29, 00054-0018, 00054-0018-20, 00054-0018-25, 00054-0018-29, 00054-0019, 00054-0019-20, 00054-0019-25, 00054-3721, 00054-3721-44, 00054-3722, 00054-3722-50, 00054-3722-63, 00054-4728, 00054-4728-25, 00054-4728-31, 00054-4741, 00054-4741-25, 00054-4741-31, 00054-4742, 00054-4742-25, 00054-8724 and 5 more
Lot numbers261739A
Expiration dates2014-10-20

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 for recall

Labeling: Missing Label; missing label on blister card

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-882-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.