Semaglutide 2.5 mg/mL pre-filled syringe recall for sterility assurance
Thrive Health Solutions is recalling Semaglutide 2.5 mg/mL pre-filled syringes (Lot #H270221) because the manufacturer cannot assure sterility of the product.
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: This is an FDA Class II recall of a sterile drug product where sterility cannot be assured. Lack of sterility in injectable medications poses risk of serious infection and potential hospitalization, meeting the Severe criteria.
Plain-English summary
Thrive Health and Wellness, LLC, dba Thrive Health Solutions, is recalling Semaglutide 2.5 mg/mL pre-filled syringes distributed nationwide. The affected lot is H270221 with an expiration date of 12/26/2025. The recall was initiated because the manufacturer lacks assurance of sterility for the product.
Patients currently using this medication should contact their healthcare provider for guidance. Do not use syringes from Lot #H270221. Contact Thrive Health Solutions or your healthcare provider with questions or to report any adverse effects.
The recalled product
- Product
- Semaglutide, 2.5 mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
- Manufacturer
- Thrive Health and Wellness, LLC, dba Thrive Health Solutions (Colorado)
- Category
- Drug — Injectable / Diabetes
- Hazard
- lack-of-sterility
- infection-risk
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 (2)
- Lot #: H270221
- Exp 12/26/2025
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- ModerateQuality Choice Earwax Removal Kit Carbamide Peroxide Subpotent Drug Recall
FDA (Drugs) · 2026-07-22
- ModerateLeader Carbamide Peroxide Earwax Removal Kit Recalled for Subpotency
FDA (Drugs) · 2026-07-22
- SevereCleviprex Injectable Emulsion Recall Due to Sterility Assurance Concerns
FDA (Drugs) · 2026-07-22
- ModerateFamily Wellness Carbamide Peroxide Earwax Removal Kit Subpotent Drug
FDA (Drugs) · 2026-07-22
- ModerateClinere Ear Wax Remover Recalled for Subpotent Carbamide Peroxide
FDA (Drugs) · 2026-07-22