KRS Global Biotechnology recalls

KRS Global Biotechnology has 129 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 9 Oct 2019. The most frequent reason is sterility.

Total recalls129since 2018

Last 12 months0reported

Class I00% of total

Ongoing0latest 9 Oct 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 129 100%Class III 0 0%

Why krs global biotechnology is recalled

Product types

By year

20198264%
20184736%

All krs global biotechnology recalls, newest first

129 total

Reported	Class	Recall	Company	Reason	Where
9 Oct 2019Drug	CLASS II	LIDOcaine HCl 2% (PF) 100 mg/ (20 mg/mL) Fill recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	Norepinephrine added to 5% Dextrose (PF) IV, 8 mg/ 032 mg/mL) recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	SUCCinylcholine Chloride (PF), 200 mg/ (20 mg/mL) Fill recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	Human Chorionic Gonadotropins Lyophilized For SC/IM Use recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	Cyclopentolate HCl 1% (5 mg/ / Phenylephrine HCl 5% 5 mg recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	Methylcobalamin Vial-For SC / IM / IV Use, 30 mg / (1 mg / mL) recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	NORepinephrine in 9% Sodium Chloride (PF) IV, 8 mg/ 032 mg/mL) recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	LIDOcaine HCl 1% (PF) 50 mg/ (10 mg/mL) Fill recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	ePHEDrine Sulfate in 9% Sodium Chloride (PF) 25 mg recalled	KRS Global Biotechnology	Sterility	Nationwide
9 Oct 2019Drug	CLASS II	L-Carnitine in a Vial, 4,590 mg/ (170 mg/mL) recalled	KRS Global Biotechnology	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.