Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fludeoxyglucose F 18 Injection USP Recalled by Petnet Solution Inc Due to cGMP Deviation
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Petnet Solution Inc directly.
Affected Products
Fludeoxyglucose F 18 Injection USP, 20-200 mCi/mL, Diagnostic - For Intravenous Use Only, Manufactured by PETNET Solutions, Inc., Knoxville, TN
Quantity: 28 doses
Why Was This Recalled?
cGMP Deviation
Where Was This Sold?
This product was distributed to 1 state: CA
About Petnet Solution Inc
Petnet Solution Inc has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report