Recalls / Brands / Buprenorphine Hydrochloride
Buprenorphine Hydrochloride
5 FDA drug recalls involving brand “Buprenorphine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 2024-05-20 | Class II | Buprenorphine Hydrochloride Injection, 0.3 mg base/mL, 1 mL Single-dose Carpuject, Sterile Cartridge Unit with | Pfizer Inc. |
| 2021-11-09 | Class II | Buprenorphine HCl, Injection, 0.3mg/mL, For Intramuscular or Intravenous Use, Rx Only, 1mL Single Dose Vial, ( | PAR Sterile Products LLC |
| 2020-08-14 | Class II | Buprenorphine HCl Injection, 0.3 mg/mL, 1 mL vial, For Intramuscular or Intravenous Use Only, Rx Only, Manufac | Hikma Pharmaceuticals USA Inc. |
| 2017-04-28 | Class II | Buprenorphine HCI Injection, 0.3 mg/mL, 1 mL Single Dose Vial (NDC 42023-179-01), packaged in 1 mL x 5 Single | PAR Sterile Products LLC |
| 2014-09-09 | Class II | Buprenorphine Hydrochloride Injection, CIII, 0.3 mg base/mL ,1 mL, 10 Carpuject Sterile Cartridge Units with | Hospira Inc. |