Semaglutide pre-filled syringe recalled due to sterility concerns
Thrive Health Solutions is recalling Semaglutide 5 mg/mL pre-filled syringes distributed nationwide because the manufacturer cannot assure the product's sterility.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The FDA classified this as Class II and the hazard is lack of assurance of sterility in an injectable drug product, which creates a direct risk of serious infection. Class II recalls with contamination or sterility risks involving injectable medications meet the Severe threshold.
Plain-English summary
Thrive Health Solutions, located in Englewood, Colorado, is recalling Semaglutide 5 mg/mL pre-filled syringes due to a lack of assurance of sterility. The affected product was distributed nationwide.
The recall involves 164 syringes with the following lot numbers and expiration dates: Lot #C03035J (exp 7/3/2025), H202959 (exp 7/6/2025), AB20N110720 (exp 7/7/2025), AB60N1121 (exp 7/7/2025), PRX022225-1 (exp 8/24/2025), and U122024 (exp 10/26/2025).
Consumers who have received this product should consult their healthcare provider. Patients should not use the product and should contact their healthcare provider or pharmacist with questions.
The recalled product
- Product
- Semaglutide, 5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
- Affected units
- 164
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (11)
- Lot #: C03035J
- Exp 7/3/2025
- H202959
- exp 7/6/2025
- AB20N110720
- exp 7/7/2025
- AB60N1121
- PRX022225-1
- exp 8/24/2025
- U122024
- exp 10/26/2025
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 14 recalled by Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado) under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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