Drug recall

ARGININE 100MG/ML (PF), 10ML Vials, MEDAUS PHARMACY

FDA recall event 74466 · Class II, Class III · Medaus, Inc.

Key facts

Event ID 74466
Recall numbers D-1167-2016, D-1168-2016, D-1169-2016, D-1170-2016, D-1171-2016, D-1172-2016, D-1173-2016, D-1174-2016, D-1175-2016, D-1176-2016, D-1177-2016, D-1178-2016 and 76 more
Recalling firm Medaus, Inc.
Product type Drugs
Products ARGININE 100MG/ML (PF), 10ML Vials, MEDAUS PHARMACY, B-COMPLEX #3 (PF), B1-100MG, B2-2-PO4-2MG, B3-100MG, B5-2MG, B6-2MG/ML, 2ML Vials, MEDAUS PHARMACY, B-COMPLEX #3 W/PRES (BENZYL ETOH 2%), B1-100MG, B2-5-PO4-2MG, B3-100MG, B5-2MG, B6-2MG/ML, 10ML Vials, MEDAUS PHARMACY, B-COMPLEX 50 IN NACL 0.9% (PF) B1-50MG, B2-5-PO4-5MG, B3-50MG, B5-50MG, B6-50MG/ML, 2ML Vials, MEDAUS PHARMACY, B-COMPLEX 50 IN NACL 0.9% W/PRES., (BENZYL ETOH 2%), B1-50MG, B2-5-PO4-5MG, B3-50MG, B5-50MG, B6-50MG/ML, 10ML Vials, MEDAUS PHARMACY and 83 more
Classification Class II, Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Lack of Assurance of Sterility
Initiation date May 13, 2016
Report date Jul 20, 2016
Termination date Jun 16, 2017
City Birmingham
State AL
Country United States
FEI number 3001298034

At a glance

  • 10–99 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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