Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II, and the presence of particulate matter in a sterile injectable product poses a significant risk of injury or adverse health consequences.
Plain-English summary
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vials. The recall was initiated because the product was found to contain particulate matter identified as nylon/polyamide and silk/proteinaceous-type material.
The affected product is Lot AC-017131 with an expiration date of 8/30/2026. The vials are prescription-only and intended for subcutaneous injection. The product was distributed nationwide within the U.S.
Consumers and healthcare providers should stop using the affected vials and contact their healthcare provider or the recalling firm for further instructions.
The recalled product
- Product
- SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
- Manufacturer
- Apollo Care, LLC
- Category
- Drug — Injectable
- Affected units
- 4,748
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: AC-017131
- Exp. 8/30/2026.
Distribution
Distributed nationwide across the United States.
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