Data Foundry

Drug recalls 2013

Ciprofloxacin Tablets — Class II drug recall D-66403-011

Terminated recall by Mylan Pharmaceuticals Inc., reported 2013-11-13, distributed nationwide. CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured accord

Recall numberD-66403-011
Product typeDrug
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmMylan Pharmaceuticals Inc., Morgantown, WV, United States
Recall initiated2013-09-13
Classified2013-11-04
Reported by FDA2013-11-13
Terminated2015-07-23
DistributedNationwide (US)
Quantity941,270 bottles
Reason classescgmp
NDC00378-7098-01
Lot numbers2002732, 2002733, 2002734, 2002735, 2002736, 2002737, 2002738, 2002739, 2002740, 2002741, 2002742, 2002743, 2002744, 2002745, 3030000, 3030001, 3030002, 3030003, 3030004, 3030005, 3030006, 3030016, 3030017, 3030018, 3030216, 3030217, 3030218, 3030219, 3030220, 3030221, 3030222, 3030223, 3030224, 3030225, 3030226, 3030227, 3030228, 3030229, 3030238, 3030351 and 26 more

Product

Ciprofloxacin Tablets, USP, 500 mg,100-count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A, NDC 0378-7098-01

Reason for recall

CGMP Deviations: Pharmaceuticals were produced and distributed with active ingredients not manufactured according to Good Manufacturing Practices.

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-66403-011. 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.