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Apotex Scientific recalls

Apotex Scientific has 3 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 20 Jul 2016. The most frequent reason is potency & assay.

Total recalls3since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 20 Jul 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 0 0%Class III 3 100%

Why apotex scientific is recalled

Potency & Assay3100%

Product types

Antidepressants3100%

By year

20163100%

All apotex scientific recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
20 Jul 2016Drug	CLASS III	Duloxetine Delayed-Release Capsules, USP, 30 mg recalled	Apotex Scientific	Potency & Assay	Nationwide
20 Jul 2016Drug	CLASS III	Duloxetine Delayed-Release Capsules, USP, 20 mg recalled	Apotex Scientific	Potency & Assay	Nationwide
20 Jul 2016Drug	CLASS III	Duloxetine Delayed-Release Capsules, USP, 60 mg recalled	Apotex Scientific	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.