Kremers Urban Pharmaceuticals recalls

Kremers Urban Pharmaceuticals has 3 recalls on record with the FDA and USDA, the earliest in 2013 and the latest reported on 22 Jul 2015. The most frequent reason is potency & assay.

Total recalls3since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 22 Jul 2015

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 3 100%Class III 0 0%

Why kremers urban pharmaceuticals is recalled

Potency & Assay267%
Other Reasons133%

Product types

By year

2015267%
2013133%

All kremers urban pharmaceuticals recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
22 Jul 2015Drug	CLASS II	Nitroglycerin Transdermal System 2 mg/hr (10 cm2) recalled	Kremers Urban Pharmaceuticals	Potency & Assay	Nationwide
22 Jul 2015Drug	CLASS II	Nitroglycerin Transdermal System 4 mg/hr (18 cm2) recalled	Kremers Urban Pharmaceuticals	Potency & Assay	Nationwide
27 Nov 2013Drug	CLASS II	Omeprazole Delayed-Release Capsules, USP, 20 mg recalledOmeprazole	Kremers Urban Pharmaceuticals	Other	KY, TN

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.