Home / Recalls / Apollo Care, LLC / D-0749-2026

D-0749-2026 Class II Ongoing

Recalled by Apollo Care, LLC — Columbia, MO

FDA drug recall D-0749-2026 was initiated by Apollo Care, LLC on Jul 29, 2026 and is designated Class II. Reason for recall: Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material The recall status is ongoing. Affected quantity: 37,546 vials.

Recall Details

Product Type: Drugs
Report Date: Aug 19, 2026
Initiation Date: Jul 29, 2026
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 37,546 vials.

Product Description

SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01

Reason for Recall

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

Distribution Pattern

Nationwide within the U.S

Code Information

Lot: C-017115, Exp. 11/25/2026; AC-017163, Exp. 12/31/2026; AC-017169, AC-017170, AC-017171, Exp. 12/31/2026; AC-017230, AC-017231, Exp. 5/5/2027.

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-0749-2026
openFDA file date: Nov 3, 2026
Loaded by RegDataLab: Nov 4, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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