Recalls / Active ingredient / Midazolam Hydrochloride
Midazolam Hydrochloride
3 FDA drug recalls involving the active ingredient “Midazolam Hydrochloride” — 1 Class I.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2017-10-27 | Class I | Midazolam Injection, USP, Preservative Free, 2 mg / 2 mL (1 mg / mL), 24 X 2mL Prefilled single-use syringes p | Fresenius Kabi USA, LLC |
| 2016-12-16 | Class II | MIDAZOLAM INJECTION, USP, *25 mg/5 mL, (5 mg/ mL), 5 mL vials, 10 Vials per carton, Rx only, APP Pharmaceutica | Fresenius Kabi USA, LLC |
| 2012-09-27 | Class II | MIDAZOLAM HYDROCHLORIDE INJECTION, 5 mg/1 mL, C-IV, For IM or IV Use, 2 mL Vials, Rx only. APP Pharmaceutical | Fresenius Kabi USA, LLC |