FDAFDA · Food and drugs·Recall number D-0058-2023
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).
Published November 16, 2022 · Recall initiated: October 7, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- OCTREOTIDE ACETATE
- Manufacturer
- Viatris Inc
- Distributor
- Nationwide in the USA
- Lot
- Lot #: AJ21002, Exp. 03/2024
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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