Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
Octreotide Acetate Injection 500 mcg/mL Recalled by Viatris Inc Due to Presence of Particulate Matter: Product complaint for the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.
Affected Products
Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes, For Subcutaneous or Intravenous Use, Rx Only, Manufactured for: Mylan Institutional LLC, Morgantown, WV 26505 U.S.A., Made in Italy, NDC: 67457-246-00 (syringe), 67457-246-01 (carton).
Quantity: 22400 syringes
Why Was This Recalled?
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris Inc
Viatris Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report