SEMAGLUTIDE 2 — Class II drug recall D-0748-2026
Ongoing recall by Apollo Care, LLC, reported 2026-08-19, distributed nationwide. Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
| Recall number | D-0748-2026 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Apollo Care, LLC, Columbia, MO, United States |
| Recall initiated | 2026-07-29 |
| Classified | 2026-08-07 |
| Reported by FDA | 2026-08-19 |
| Distributed | Nationwide (US) |
| Quantity | 23,029 vials |
| Reason classes | specification failure |
| NDC | 71170-0811-02 |
| Lot numbers | AC-017114, AC-017164, AC-017204, AC-017205 |
| Expiration dates | 2026-11-24, 2026-12-31 |
Product
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
Reason for recall
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0748-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.