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Moderate recall: A hazard has been identified, with no injuries reported yet. Follow the steps below.

Siegfried Barbera, SL 2023-12-20 Health moderate FDA
Health · FDA · Recall #FDA-D-0149-2024

Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried… Recall

Issued December 20, 2023 · Siegfried Barbera, SL

In December 2023, Siegfried Barbera, SL recalled the Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried…, a moderate health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Failed Dissolution Specifications

What you should do

  1. 1 Stop using Votrient (pazopanib) 200 mg tablets, 120-count bottle, Rx Only, Manufactured by: Siegried… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Siegfried Barbera, SL to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Siegfried Barbera, SL
Category
Health
Recall date
December 20, 2023
Units affected
Not reported
Sold at
Nationwide
Recall number
FDA-D-0149-2024
Made in
Spain
Issuing agency
FDA

In context

  • Siegfried Barbera, SL has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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