D-0058-2023 Class I Terminated
Recall Details
- Product Type
- Drugs
- Report Date
- November 16, 2022
- Initiation Date
- October 7, 2022
- Termination Date
- January 12, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 22400 syringes
Product Description
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).
Reason for Recall
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Distribution Pattern
Nationwide in the USA
Code Information
Lot #: AJ21002, Exp. 03/2024