FDA Drug recall · Reported August 19, 2026
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Apollo Care, LLC recalled SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous In… - a moderate-severity action.
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous In… was recalled by Apollo Care, LLC in August 19, 2026. Reason: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material. Check the official notice for the remedy. Verify recall #D-0747-2026 with the FDA Drug before acting.
The recall
Apollo Care, LLC issued this moderate-severity FDA Drug recall-Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material.
- Moderate
- severity level
- Class II
- classification
- August 19, 2026
- reported
Sourced from official FDA Drug enforcement records. Verify recall #D-0747-2026 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Drug action (record #D-0747-2026) was formally reported on August 19, 2026, with the manufacturer initiating the action on July 29, 2026. It is classified under Moderate severity (Class II), with a current status of Ongoing. Apollo Care, LLC is listed as the recalling firm, operating out of Columbia, MO. Federal records list the affected scope as 56,918 vials..
The documented reason for this recall is: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material Distribution data in the federal record shows the product reached: Nationwide within the U.S. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Drug and 2 from Apollo Care, LLC - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Drugs & Medications recalls over time
Where this recall sits in its category - 14,472 drugs & medications recalls on record
Of 88,244 recalls with an agency hazard classification, 19,068 are high severity, 64,652 moderate, and 4,524 low. A further 16,179 CPSC/NHTSA recalls have no agency class and are excluded from this split. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Product description
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
Reason for recall
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Ongoing |
| Recall number | D-0747-2026 |
| Date reported | August 19, 2026 |
| Date initiated | July 29, 2026 |
| Recalling firm | Apollo Care, LLC |
| Firm location | Columbia, MO |
| Affected scope | 56,918 vials. |
| Distribution | Nationwide within the U.S |
Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (D-0747-2026) and product description against the item you own. Search the archive
- Confirm the current status with FDA Drug before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
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Nationwide recalls with similar severity or category timing
Drug and device notices outside this firm and state, matched by severity timing and product category.
Similar severity · nearest report date
Same archive severity grade (Moderate), closest by report date among other firms and states.
Similar Drugs & Medications · nearest report date
Same product category, closest by report date among other firms and states (deduped against the severity set).
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Methodology · Corrections · Archive as of August 2026