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Endo Usa, Inc.

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 2026-05-20

Crystallization; identified as Buprenorphine free base

Buprenorphine Hydrochloride, Injection, 0.3mg/mL, 5x1 mL Single Dose Vials, Rx only, Manufactured for: Endo USA, Malvern, PA 19855, NDC 42023-179-05.

Check these codes: Lot #: 84132, Exp 02/28/2027; 87693, Exp 03/31/2027

34,293 vials · distributed usa nationwide Recall D-0527-2026 on FDA.gov ↗
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