Apollo Care Semaglutide Recall: FDA Class II

Why it was recalled

Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material

Product description

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

Lot numbers, UPCs & expiration codes

Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.

Where it was sold

Nationwide within the U.S

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0748-2026
Classification: Class II
Status: Ongoing
Recall initiated: Jul 29, 2026
FDA report date: Aug 19, 2026
Quantity: 23,029 vials.
Recall type: Voluntary: Firm initiated
Recalling firm: Apollo Care, LLC

Original FDA data

Every field from FDA enforcement report D-0748-2026, exactly as published.

Show all FDA fields

City: Columbia
State: MO
Status: Ongoing
Country: United States
Event ID: 99505
Address: 3801 Mojave Ct Ste 101
Code information: Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.
Postal code: 65202-4042
Report date: Aug 19, 2026
Product type: Drugs
Recall number: D-0748-2026
Classification: Class II
Recalling firm: Apollo Care, LLC
Product quantity: 23,029 vials.
Reason for recall: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
Voluntary / mandated: Voluntary: Firm initiated
Product description: 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
Distribution pattern: Nationwide within the U.S
Recall initiation date: Jul 29, 2026
Initial firm notification: E-Mail
Center classification date: Aug 7, 2026

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0748-2026, published Aug 19, 2026. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 6, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

Apollo Care Semaglutide 2 Recall

Summary