Lisinopril And Hydrochlorothiazide recalls

Lisinopril And Hydrochlorothiazide products have been recalled 5 times, most recently on 23 Jul 2025. The recalling company is usually Lupin Pharmaceuticals. The most common reason is manufacturing (cgmp) deviations.

Total recalls5since 2016

Last 12 months0reported

Class I00% of total

Ongoing1latest 23 Jul 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 1Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 4 80%Class III 1 20%

Why lisinopril and hydrochlorothiazide is recalled

Companies

Lupin Pharmaceuticals480%
Cardinal Healthcare120%

Product types

Blood Pressure Medication5100%

By year

2025120%
2024120%
2019240%
2016120%

Ongoing lisinopril and hydrochlorothiazide recalls

1 active

Reported	Class	Recall	Company	Reason	Where
23 Jul 2025Drug	CLASS II	Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg recalledLisinopril And Hydrochlorothiazide	Lupin Pharmaceuticals	Packaging Defects	Nationwide

All lisinopril and hydrochlorothiazide recalls, newest first

5 total

Reported	Class	Recall	Company	Reason	Where
23 Jul 2025Drug	CLASS II	Lisinopril and Hydrochlorothiazide Tablets USP 20mg/12.5mg recalledLisinopril And Hydrochlorothiazide	Lupin Pharmaceuticals	Packaging Defects	Nationwide
3 Jan 2024Drug	CLASS II	Lisinopril and Hydrochlorothiazide Tablets USP, 10mg/12.5mg recalledLisinopril And Hydrochlorothiazide	Cardinal Healthcare	Manufacturing (CGMP) Deviations	Nationwide
21 Aug 2019Drug	CLASS II	Lisinopril and Hydrochlorothiazide Tablets USP, 10 mg/12.5 mg recalledLisinopril And Hydrochlorothiazide	Lupin Pharmaceuticals	Other	Nationwide
31 Jul 2019Drug	CLASS II	Lisinopril and Hydrochlorothiazide Tablets USP, 20 mg/12.5 mg recalledLisinopril And Hydrochlorothiazide	Lupin Pharmaceuticals	Other	Nationwide
6 Jul 2016Drug	CLASS III	Lisinopril & Hydrochlorothiazide Tables, USP 20mg/12.5mg recalledLisinopril And Hydrochlorothiazide	Lupin Pharmaceuticals	Manufacturing (CGMP) Deviations	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.