The Recall Desk
HighFDA (Drugs)·D-0404-2026·Announced 2026-04-01

[pending] OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)

Pending LLM rewrite. Source: FDA_DRUG D-0404-2026.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: Pending LLM scoring against the rubric.

Plain-English summary

Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.

The recalled product

Product
OCTREOTIDE ACETATE (OCTREOTIDE ACETATE)
Brand
OCTREOTIDE ACETATE
Manufacturer
Teva Pharmaceuticals USA, Inc

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (4)

  • Lot: 4401619
  • Exp.: 09/30/2026
  • 4501005
  • 03/31/2027.

Distribution

Distributed nationwide across the United States.

Same brand · OCTREOTIDE ACETATE