RecallRadar

FDA Drug recall D-0970-2018

Solco Healthcare US Valsartan, USP, 160 MG Tablets, 90-count bottles, Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd

On 2018-08-01 the FDA classified a Class II recall of Solco Healthcare US Valsartan, USP, 160 MG Tablets, 90-count bottles, Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd by Prinston Pharmaceutical, citing CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0970-2018
ClassificationClass II
Statusongoing
Initiated2018-07-13
Published2018-08-01
Last updated2026-09-13 11:52 UTC
CompanyPrinston Pharmaceutical
Distributionn/a

Product

Solco Healthcare US Valsartan, USP, 160 MG Tablets, 90-count bottles, Rx Only Manufactured by: Zhejiang Huahai Pharmaceutical Co., Ltd. Xynqiao, Linhai, Zhejiang 317024, China Distributed by: Solco Healthcare US, LLC Cranbury, NJ 08512 USA NDC 43547-369-09

Reason

CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.

Identifiers

ndc43547-367-03
ndc43547-367-09
ndc43547-367-50
ndc43547-367-11
ndc43547-368-03
ndc43547-368-09
ndc43547-368-50
ndc43547-368-11
ndc43547-369-03
ndc43547-369-09
ndc43547-369-50
ndc43547-369-11
ndc43547-370-03
ndc43547-370-09
ndc43547-370-50
ndc43547-370-11
code_infoAll lots within expiry.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0970-2018%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.