Class II

Drug Recall: Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or Intravenous use, Manufactured for: Endo USA, Malvern, PA 19355, NDC 42023-179-05

Par Health USA, LLC · June 12, 2026

Reason for Recall

Crystallization; identified as Buprenorphine free base

Distribution

Nationwide in the USA.

States Affected

NATIONWIDE

Quantity Affected

46,334 units

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0596-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Par Health USA, LLC Drug Recall: Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or Intravenous use, Manufactured for: Endo USA, Malvern, PA 19355, NDC 42023-179-05 | SafeCheck