Bupropion Hydrochloride recalls

Bupropion Hydrochloride products have been recalled 16 times, most recently on 29 Oct 2025. The recalling company is usually Sun Pharmaceutical Industries. The most common reason is potency & assay.

Total recalls16since 2014

Last 12 months1reported

Class I00% of total

Ongoing3latest 29 Oct 2025

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 1 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 6 38%Class III 10 63%

Why bupropion hydrochloride is recalled

Companies

Product types

Antidepressants16100%

By year

202516%
2024213%
2023425%
2022213%
202116%
201816%
201716%
2016213%
201516%
201416%

Ongoing bupropion hydrochloride recalls

3 active

Reported	Class	Recall	Company	Reason	Where
29 Oct 2025Drug	CLASS II	Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg recalledBupropion Hydrochloride	Graviti Pharmaceuticals Private	Other	Nationwide
17 Jul 2024Drug	CLASS II	buPROPion Hydrochloride Extended-release Tablets recalledBupropion Hydrochloride	Amerisource Health Services	Potency & Assay	Nationwide
17 Jan 2024Drug	CLASS II	buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg recalledBupropion Hydrochloride	Rising Pharma Holding	Other	Nationwide

All bupropion hydrochloride recalls, newest first

16 total

Reported	Class	Recall	Company	Reason	Where
29 Oct 2025Drug	CLASS II	Bupropion Hydrochloride Extended-Release Tablets USP (XL), 300 mg recalledBupropion Hydrochloride	Graviti Pharmaceuticals Private	Other	Nationwide
17 Jul 2024Drug	CLASS II	buPROPion Hydrochloride Extended-release Tablets recalledBupropion Hydrochloride	Amerisource Health Services	Potency & Assay	Nationwide
17 Jan 2024Drug	CLASS II	buPROPion Hydrochloride Extended-Release Tablets, USP (XL) 150mg recalledBupropion Hydrochloride	Rising Pharma Holding	Other	Nationwide
13 Dec 2023Drug	CLASS III	buPROPion Hydrochloride Extended-Release Tablets, USP (SR) 200 mg recalledBupropion Hydrochloride	SUN Pharmaceutical Industries	Potency & Assay	Nationwide
25 Oct 2023Drug	CLASS III	Bupropion Hydrochloride Extended-Release Tablets USP (SR), 150 mg recalledBupropion Hydrochloride	SUN Pharmaceutical Industries	Potency & Assay	Nationwide
31 May 2023Drug	CLASS II	buPROPrion Hydrochloride Extended-Release Tablets, USP (SR) 150 mg recalledBupropion Hydrochloride	SUN Pharmaceutical Industries	Potency & Assay	Nationwide
22 Feb 2023Drug	CLASS II	BuPROPion Hydrochloride Tablets, USP 75 mg (10 recalledBupropion Hydrochloride	Amerisource Health Services	Potency & Assay	Nationwide
18 May 2022Drug	CLASS III	buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 150 mg recalledBupropion Hydrochloride	SUN Pharmaceutical Industries	Packaging Defects	Nationwide
18 May 2022Drug	CLASS III	buPROPion Hydrochloride Extended-Release Tablet, USP (SR), 200 mg recalledBupropion Hydrochloride	SUN Pharmaceutical Industries	Other	Nationwide
2 Jun 2021Drug	CLASS II	bupropion Hydrochloride Tablets, USP 75 mg recalled by Cardinal HealthBupropion Hydrochloride	Cardinal Health	Manufacturing (CGMP) Deviations	FL, GA, SC
26 Sep 2018Drug	CLASS III	Bupropion Hydrochloride ER Tablets, USP 150 mg recalledBupropion Hydrochloride	InvaGen Pharmaceuticals	Potency & Assay	Nationwide
1 Feb 2017Drug	CLASS III	buPROPion Hydrochloride Extended-release Tablets, USP (SR) recalledBupropion Hydrochloride	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
12 Oct 2016Drug	CLASS III	buPROPion Hydrochloride Extended-release Tablets, USP (SR) recalledBupropion Hydrochloride	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
27 Jul 2016Drug	CLASS III	buPROPion Hydrochloride Extended Release Tablets USP (SR) 150 mg recalledBupropion Hydrochloride	Sun Pharmaceutical Industries	Potency & Assay	Nationwide
26 Aug 2015Drug	CLASS III	buPROPion Hydrochloride Extended-¿release Tablets USP (SR) recalledBupropion Hydrochloride	Sun Pharma Global Fze	Potency & Assay	Nationwide
5 Feb 2014Drug	CLASS III	BuPROPion Hydrochloride Extended-Release Tablet (XL) 150mg recalledBupropion Hydrochloride	Actavis	Potency & Assay	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.