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

Severity split

Class I 0 0%Class II 129 100%Class III 0 0%

Why krs global biotechnology is recalled

By year

All krs global biotechnology recalls, newest first

129 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IILIDOcaine HCl 2% (PF) 100 mg/ (20 mg/mL) Fill recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IINorepinephrine added to 5% Dextrose (PF) IV, 8 mg/ (0.032 mg/mL) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IISUCCinylcholine Chloride (PF), 200 mg/ (20 mg/mL) Fill recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIHuman Chorionic Gonadotropins Lyophilized For SC/IM Use recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IICyclopentolate HCl 1% (5 mg/ / Phenylephrine HCl recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIMethylcobalamin Vial-For SC / IM / IV Use, 30 mg / (1 mg / mL) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IINORepinephrine in 0.9% Sodium Chloride (PF) IV, 8 mg/ (0.032 mg/mL) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IILIDOcaine HCl 1% (PF) 50 mg/ (10 mg/mL) Fill recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIePHEDrine Sulfate in 0.9% Sodium Chloride (PF) 25 mg recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIL-Carnitine in a Vial, 4,590 mg/ (170 mg/mL) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIPHENYephrine HCl in 0.9% Sodium Chloride (PF) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIMagnesium Chloride Hexahydrate 82.5 mg/mL recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIPHENYephrine HCl in 0.9% Sodium Chloride (PF) (Contains Sulfites) recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIHuman Chorionic Gonadotropins Lyophilized For SC/IM Use recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIKetamine in 0.9% Sodium Chloride (PF) 50 mg recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IISermorelin 9 mg / GHRP6, 5.4 mg / GHRP2, 5.4 mg recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IICyclopentolate HCl 1% (10 mg/mL) / Phenylephrine HCl recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIL-Asparaginase Lyophilized, 10,000 International Units/Vial recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIVitamin 10 D Lyophilized, Vial For IM/Slow IV Infusion Use recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIGlutathione Vial-For IM Use-Hypertonic solution, 6,000 mg recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIQuadmix #13A (Prostaglandin E1-0.3 mg / Papaverine HCl recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIVitamin 9 Lyophilized, Vial For IM Use recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIAlpha Lipoic Acid (PF) 750 mg recalled by KRS Global BiotechnologyKRS Global BiotechnologySterilityNationwide
DrugCLASS IISermorelin Acetate 9 mg / Vial, For SC Use-Lyophilized recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IILidocaine HCl 30 mg/mL/Hyaluronidase/mL (PF) Fill recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IISermorelin Acetate, 3 mg/mL/GHRP6, 1.8 mg/mL/GHRP2 recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIPHENYLephrine HCl in 0.9% Sodium Chloride (PF), 1 mg recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IIMoxifloxacin 0.1% in BSS, Ophthalmic Injection recalledKRS Global BiotechnologySterilityNationwide
DrugCLASS IILIDOcaine 2% (20 mg/mL)/Bupivacaine recalled by KRS Global BiotechnologyKRS Global BiotechnologySterilityNationwide
DrugCLASS IISermorelin Acetate, 9 mg / Ghrp recalled by KRS Global BiotechnologyKRS Global BiotechnologySterilityNationwide

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.