Data Foundry

Drug recalls 2020

Clonidine Hydrochloride Tablets — Class III drug recall D-0829-2020

Terminated recall by UNICHEM PHARMACEUTICALS USA INC, reported 2020-02-12, distributed nationwide. Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to poten

Recall numberD-0829-2020
Product typeDrug
ClassificationClass III
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmUNICHEM PHARMACEUTICALS USA INC, East Brunswick, NJ, United States
Recall initiated2020-01-29
Classified2020-02-06
Reported by FDA2020-02-12
Terminated2021-01-08
DistributedNationwide (US)
Quantity19,161,600 units
Reason classeslabeling, specification failure
NDC29300-0135, 29300-0135-01, 29300-0135-05, 29300-0135-10, 29300-0135-50, 29300-0136, 29300-0136-01, 29300-0136-05, 29300-0136-10, 29300-0136-50, 29300-0137, 29300-0137-01, 29300-0137-05, 29300-0137-10, 29300-0137-25, 29300-0468, 29300-0468-01, 29300-0468-05, 29300-0468-10, 29300-0468-50
Lot numbersGCLL18108, GCLL18109, GCLL18110, GCLL19003
Expiration dates2020-10-31, 2020-12-31

Product

Clonidine Hydrochloride Tablets, USP 0.1mg, Rx Only, 100-count bottle, Manufactured by: Unichem Laboratories Ltd. Pilerne Ind. Estate, Pilerne Bardez, Goa 403 511 India. Manufactured for: Unichem Pharmaceuticals (USA), Inc. East Brunswick, NJ 08816. NDC 29300-135-01

Reason for recall

Failed Impurities/Degredation Specifications: This recall is initiated as a precautionary measure due to potential migration of Benzophenone at very low level into product from container 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-0829-2020. 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.