Attix Pharmaceuticals recalls

Attix Pharmaceuticals has 471 recalls on record with the FDA and USDA, the earliest in 2015 and the latest reported on 29 Jun 2016. The most frequent reason is packaging defects.

Total recalls471since 2015

Last 12 months0reported

Class I00% of total

Ongoing0latest 29 Jun 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 470 100%Class III 1 0%

Why attix pharmaceuticals is recalled

Product types

By year

201610%
2015470100%

All attix pharmaceuticals recalls, newest first

471 total

Reported	Class	Recall	Company	Reason	Where
29 Jun 2016Drug	CLASS III	Mycophenolate Mofetil, Bulk Powder, Quantity recalled	Attix Pharmaceuticals	Manufacturing (CGMP) Deviations	CO
29 Apr 2015Drug	CLASS II	Miltefosine active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Azithromycin Dihydrate active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Bromocriptine Mesylate active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Droperidol active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Meloxicam active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Isoproterenol Hydrochloride active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Hydralazine HCl active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Atazanavir active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	Nationwide
29 Apr 2015Drug	CLASS II	Monobenzone active pharmaceutical ingredient recalled	Attix Pharmaceuticals	Packaging Defects	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.