Wells Pharmacy Network recalls

Wells Pharmacy Network has 104 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 11 Jan 2017. The most frequent reason is sterility.

Total recalls104since 2016

Last 12 months0reported

Class I00% of total

Ongoing0latest 11 Jan 2017

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 100 96%Class III 4 4%

Why wells pharmacy network is recalled

Sterility9793%
Potency & Assay77%

Product types

By year

20179793%
201677%

All wells pharmacy network recalls, newest first

104 total

Reported	Class	Recall	Company	Reason	Where
11 Jan 2017Drug	CLASS II	Alprostadil 40 mcg/mL Injectable vials recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Testosterone Enanthate in Grapeseed Oil Injectable recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	QUAD2 (Pap/Phen/Alpros/Atro) 9 mg/1 mg/10 mg/0.1 mg/mL recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Trimix Injectable 30 mg/3 mg/60 mcg/mL, a), b) and c) vials recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Methylcobalamin Injectable (Dr recalled by Wells Pharmacy Network	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Trimix Injectable 65 mg/0.59 mg/5.9 mcg/mL a), b) recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Testosterone Cypionate in Sesame Oil Injectable, (NY State) recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Indocyanine Green (P.F.), 15 mg Injectable Kit recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Bimix 30 mg/1 mg/mL Injectable, a) and b) vial recalled	Wells Pharmacy Network	Sterility	Nationwide
11 Jan 2017Drug	CLASS II	Sermorelin Acetate/GHRP 6 mg/3 mg Injectable Kit recalled	Wells Pharmacy Network	Sterility	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.