Amedra Pharmaceuticals recalls

Amedra Pharmaceuticals has 4 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 1 Jan 2014. The most frequent reason is potency & assay.

Total recalls4since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 1 Jan 2014

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 4 100%Class III 0 0%

Why amedra pharmaceuticals is recalled

Potency & Assay4100%

Product types

ADHD Medication4100%

By year

2014125%
2013375%

All amedra pharmaceuticals recalls, newest first

4 total

Reported	Class	Recall	Company	Reason	Where
1 Jan 2014Drug	CLASS II	Dexedrine¿ (Dextroamphetamine Sulfate) Spansules¿ recalled	Amedra Pharmaceuticals	Potency & Assay	Nationwide
6 Mar 2013Drug	CLASS II	Dextroamphetamine Sulfate Extended Release Capsules, 5 mg recalled	Amedra Pharmaceuticals	Potency & Assay	Nationwide
6 Mar 2013Drug	CLASS II	Dextroamphetamine Sulfate Extended Release Capsules, 5 mg recalled	Amedra Pharmaceuticals	Potency & Assay	Nationwide
6 Mar 2013Drug	CLASS II	Dextroamphetamine Sulfate Extended Release Capsules, 5 mg recalled	Amedra Pharmaceuticals	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.