Class I
Terminated
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).
This recall has been terminated (originally issued November 16, 2022).
- Company
- Viatris Inc
- Recall Initiated
- October 7, 2022
- Posted
- November 16, 2022
- Recall Number
- D-0058-2023
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 22400 syringes
- Firm Location
- Canonsburg, PA, United States
- Official Source
- View on FDA website ↗
Reason for Recall
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Distribution
Nationwide in the USA
Lot / Code Info
Lot #: AJ21002, Exp. 03/2024
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