Viatris recalls 10x1mL Octreotide syringes due to glass particles. Stop using if you have these syringes before expiration.
Presence of Particulate Matter: Product complaint for the presence of glass particles in a syringe.
Viatris is recalling 10 single-dose syringes of Octreotide Acetate Injection because they contain glass particles. This could cause injury if injected.
Glass particles in the syringe could cause injury when injected. This is a product complaint from users, not a confirmed safety issue.
People with prescriptions for Octreotide Acetate Injection 500 mcg/mL syringes. Those using the product for medical treatment are most at risk.
Check for syringes labeled 'Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes'. They were made in Italy with NDC 67457-246-00 (syringe) and 67457-246-01 (carton).
Look for the NDC numbers 67457-246-00 (syringe) and 67457-246-01 (carton) on the product.
If you have the recalled syringes, stop using them immediately to avoid potential injury from glass particles.
The recall is due to a product complaint about glass particles in the syringes.
Check for syringes labeled 'Octreotide Acetate Injection 500 mcg/mL, 10 x 1 mL Single-Dose Unit-of-Use Syringes' with NDC numbers 67457-246-00 (syringe) and 67457-246-01 (carton).
The recall record does not specify a return process or deadline.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0058-2023 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0058-2023 from Viatris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
