Par Health Usa, LLC — Buprenorphine HCl recall — Check your batch

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Par Health Usa, LLC

Check your batch

Check the batch codes below. If yours matches, return it for a refund rather than take it.

Class II

May cause temporary or medically reversible harm. Serious consequences are unlikely.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check your batch Filed 2026-06-24

Crystallization; identified as Buprenorphine free base

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

Check these codes: Lot #: 82886, exp 09/30/2026; 89646, exp 05/31/2027

46,334 units · distributed nationwide in the usa. Recall D-0596-2026 on FDA.gov ↗

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