Teva North America recalls

Teva North America has 12 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 12 Oct 2016. The most frequent reason is potency & assay.

Total recalls12since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 12 Oct 2016

Recalls per month, last 24 months

click a bar for that month

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

Severity split

Class I 0 0%Class II 8 67%Class III 4 33%

Why teva north america is recalled

Product types

Brands

Amoxicillin18%
Capecitabine18%

By year

201612100%

All teva north america recalls, newest first

12 total

Reported	Class	Recall	Company	Reason	Where
12 Oct 2016Drug	CLASS III	Claravis (isotretinoin capsules USP), 10mg recalled	Teva North America	Potency & Assay	Nationwide
14 Sep 2016Drug	CLASS II	Ondansetron Injection USP 40 mg/ (2 mg/mL) recalled	Teva North America	Manufacturing (CGMP) Deviations	Nationwide
14 Sep 2016Drug	CLASS II	Eptifibatide Injection 75 mg/ (0.75 mg/mL) single use vial recalled	Teva North America	Manufacturing (CGMP) Deviations	Nationwide
14 Sep 2016Drug	CLASS II	Linezolid Injection 600 mg recalled by Teva North America	Teva North America	Manufacturing (CGMP) Deviations	Nationwide
14 Sep 2016Drug	CLASS II	Argatroban Injection in 0.9% Sodium Chloride 250 mg/ (1 mg/mL) recalled	Teva North America	Manufacturing (CGMP) Deviations	Nationwide
31 Aug 2016Drug	CLASS II	Amoxicillin for Oral Suspension USP, 400 mg recalledAmoxicillin	Teva North America	Potency & Assay	Nationwide
17 Aug 2016Drug	CLASS II	Albuterol Sulfate Syrup, 2 mg recalled by Teva North America	Teva North America	Particulate Matter	Nationwide
10 Aug 2016Drug	CLASS III	Children's Qnasl 40 mcg (beclomethasone dipropionate) Nasal recalled	Teva North America	Potency & Assay	Nationwide
3 Aug 2016Drug	CLASS III	mitoXANTRONE Injection USP (concentrate), 20 mg recalled	Teva North America	Potency & Assay	Nationwide
3 Aug 2016Drug	CLASS III	Divalproex Sodium Delayed-release Tablets USP, RX, 250 mg recalled	Teva North America	Other	Nationwide
1 Jun 2016Drug	CLASS II	Linezolid Injection, 600 mg/ Single use container bags recalled	Teva North America	Sterility	Nationwide
9 Mar 2016Drug	CLASS II	Capecitabine tablets USP 500 mg, Cytotoxic Agent recalledCapecitabine	Teva North America	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.