Data Foundry

Drug recalls 2014

Human Chorionic Gonadotropin — Class I drug recall D-1263-2014

Terminated recall by Medisca Inc., reported 2014-05-07, distributed nationwide. Labeling: Label Error on Declared Strength; Firm states that erroneous potency information was found on the la

Recall numberD-1263-2014
Product typeDrug
ClassificationClass I
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMedisca Inc., Irving, TX, United States
Recall initiated2013-10-21
Classified2014-04-25
Reported by FDA2014-05-07
Terminated2016-11-16
DistributedNationwide (US)
Quantity296 units
Reason classeslabeling, potency
NDC38779-2673-01, 38779-2673-02, 38779-2673-06
Lot numbers05/16, 101751/A, 101752/A, 101799/A, 9002-61-3

Product

Human Chorionic Gonadotropin, EP (HCG) in 5 mu. 2 mu, and 1 mu packages, For use and distribution in prescription compounding, manufacturing, processing or repacking only in accordance with FDA regulations and applicable law. Potency 5489.6IU/mg. Packed by Medisca, Inc. Irving, TX, 75063, USA NDC 38779-2673-1, NDC 38779-2673-2, and NDC 38779-2673-6. Lot Numbers 101751/A, Exp: 05/16, CAS: 9002-61-3; 101752/A, Exp: 05/16, CAS 9002-61-3; and 101799/A, Exp: 05/16, CAS: 9002-61-3

Reason for recall

Labeling: Label Error on Declared Strength; Firm states that erroneous potency information was found on the label.

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-1263-2014. 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.