First Pharma Associates recalls

First Pharma Associates has 18 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 17 Jul 2019. The most frequent reason is sterility.

Total recalls18since 2019

Last 12 months0reported

Class I00% of total

Ongoing0latest 17 Jul 2019

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 18 100%Class III 0 0%

Why first pharma associates is recalled

Sterility18100%

Product types

Injectable & IV Drugs1794%
Eye Drops16%

By year

201918100%

All first pharma associates recalls, newest first

18 total

Reported	Class	Recall	Company	Reason	Where
17 Jul 2019Drug	CLASS II	Hydroxocobalamin 10 mg/mL Injection (ALT) Solution vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Hydroxyprogesterone Caproate 250 mg/mL Sesame Oil Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Methylcobalamin 1 mg/mL Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Chorionic Gonadotropin 2,000U/mL PF Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Testosterone Cypionate 200 mg/mL Ethyl Oleate Injection recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Serum Tears 20% Eye Drops PF Solution recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	PAP/PHEN/PGE1 18 mg/0.6mg/5.88mcg/mL Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	PAP/PHEN/PGE1 30 mg/2mg/20mcg/mL Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Testosterone Cypionate 100 mg/mL Sesame Oil Injection vial recalled	First Pharma Associates	Sterility	ID, WA
17 Jul 2019Drug	CLASS II	Testosterone Cyp/Estradiol Cyp 50 mg/2.5 mg/mL Injection vial recalled	First Pharma Associates	Sterility	ID, WA

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.