Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fludeoxyglucose F 18 Injection Recalled by The General Hospital Corporation Due to Lack of Assurance of Sterility
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 The General Hospital Corporation directly.
Affected Products
Fludeoxyglucose F 18 Injection, 20-300 mCi/mL at End of Synthesis (EOS) Solution, 50 mL glass vial, Rx only, Manufactured by Massachusetts General Hospital PET Center, Boston, MA NDC 76318-334-50
Quantity: 50 mL vial
Why Was This Recalled?
Lack of Assurance of Sterility
Where Was This Sold?
Product was distributed to one direct account.
About The General Hospital Corporation
The General Hospital Corporation 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