Sun Pharma Global Fze recalls

Sun Pharma Global Fze has 4 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 9 Mar 2016. The most frequent reason is potency & assay.

Total recalls4since 2015

Last 12 months0reported

Class I00% of total

Ongoing0latest 9 Mar 2016

Recalls per month, last 24 months

click a bar for that month

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

Severity split

Class I 0 0%Class II 3 75%Class III 1 25%

Why sun pharma global fze is recalled

Potency & Assay375%
Particulate Matter125%

Product types

By year

2016125%
2015375%

All sun pharma global fze recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
9 Mar 2016Drug	CLASS II	Alendronate Sodium Tablets, USP, 70 mg* blisters recalled	Sun Pharma Global Fze	Potency & Assay	Nationwide
26 Aug 2015Drug	CLASS III	buPROPion Hydrochloride Extended-¿release Tablets USP (SR) recalledBupropion Hydrochloride	Sun Pharma Global Fze	Potency & Assay	Nationwide
4 Mar 2015Drug	CLASS II	Ketorolac Tromethamine Ophthalmic Solution recalled	Sun Pharma Global Fze	Particulate Matter	Nationwide
18 Feb 2015Drug	CLASS II	Levetiracetam, extended release tablets, 750 mg recalled	Sun Pharma Global Fze	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.