Apollo Care recall: Semaglutide 12.5MG and 10 more products
Apollo Care, LLC is recalling Semaglutide 12.5MG and 10 more products – 56,918 vials.; 23,029 vials.; 37,546 vials.; 9,762 vials.; 24,608 vials.; 4,748 vials.; 250 vials.; 500 vials.; 4,250 vials.. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on July 29, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Semaglutide 12.5MG and 10 more products |
| Brand | Apollo Care |
| Company | Apollo Care, LLC |
| Type | Drugs |
| Classification | Class II |
| Recall date | July 29, 2026 |
| Published by FDA | August 19, 2026 |
| Quantity | 56,918 vials.; 23,029 vials.; 37,546 vials.; 9,762 vials.; 24,608 vials.; 4,748 vials.; 250 vials.; 500 vials.; 4,250 vials. |
| Recall ID | 99505 |
Recalled products (11)
- 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
- FDA recall number
- D-0747-2026
- Codes, lots and dates
- Lot: AC-017108, Exp. 11/17/2026; AC-017110, Exp. 11/20/2026; AC-017112, Exp. 11/21/2026; AC-017142, AC-017144, Exp. 12/10/2026; AC-017166, AC-017167, AC-017177, AC-017213, AC-017224, AC-017225, Exp. 12/31/2026
- Quantity
- 56,918 vials.
- Classification
- Class II
- 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
- FDA recall number
- D-0748-2026
- Codes, lots and dates
- Lot: AC-017114, Exp. 11/24/2026; AC-017164, AC-017204, AC-017205, Exp. 12/31/2026.
- Quantity
- 23,029 vials.
- Classification
- Class II
- 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
- FDA recall number
- D-0749-2026
- Codes, lots and dates
- 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.
- Quantity
- 37,546 vials.
- Classification
- Class II
- SEMAGLUTIDE 4.5mg (0.9 mg/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-812-03
- FDA recall number
- D-0750-2026
- Codes, lots and dates
- Lot: AC-017124, Exp. 8/30/2026; AC-017136, Exp. 12/31/2026.
- Quantity
- 9,762 vials.
- Classification
- Class II
- SEMAGLUTIDE 9mg (4.5 mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-822-02
- FDA recall number
- D-0751-2026
- Codes, lots and dates
- Lot: AC-017125, Exp. 8/30/2026; AC-017138, AC-017147, AC-017214, AC-017226, AC-017228, Exp. 12/31/2026.
- Quantity
- 24,608 vials.
- Classification
- Class II
- 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
- FDA recall number
- D-0752-2026
- Codes, lots and dates
- Lot: AC-017131, Exp. 8/30/2026.
- Quantity
- 4,748 vials.
- Classification
- Class II
- SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
- FDA recall number
- D-0753-2026
- Codes, lots and dates
- Lot: AC-017271, Exp. 12/12/2026.
- Quantity
- 250 vials.
- Classification
- Class II
- SEMAGLUTIDE 5mg (1mg/mL), Glycine 25 mg (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 71170-712-03
- FDA recall number
- D-0754-2026
- Codes, lots and dates
- Lot: AC-017272, Exp. 12/12/2026.
- Quantity
- 250 vials.
- Classification
- Class II
- SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/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 71170-721-01
- FDA recall number
- D-0755-2026
- Codes, lots and dates
- Lot: AC-017273, Exp. 12/12/2026.
- Quantity
- 250 vials.
- Classification
- Class II
- SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02
- FDA recall number
- D-0756-2026
- Codes, lots and dates
- Lot: AC-017274, Exp. 12/12/2026.
- Quantity
- 500 vials.
- Classification
- Class II
- SEMAGLUTIDE 20mg (5mg/mL), Glycine 20 mg (5mg/mL), 4 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-724-04.
- FDA recall number
- D-0757-2026
- Codes, lots and dates
- Lot: AC-017275, Exp. 12/13/2026; AC-017282, AC-017285, Exp. 12/27/2026.
- Quantity
- 4,250 vials.
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99505
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Columbia, MO, United States
Why it was recalled
The reason the FDA lists: “Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material”
Where it was sold
Nationwide. Distribution as the FDA records it: “Nationwide within the U.S”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99505, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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| Oct 7, 2026 | Aurolab Trust recall: FOCUS PI Hypromellose 0.7% FormulaDrugs · 25,220 bottles | a sterility problem Serious | FDA Class II |
| Oct 7, 2026 | Amneal Pharmaceuticals recall: Estradiol GelDrugs · 2,592 30-count cartons | Defective Container; packets were found to be either empty or partially full. Serious | FDA Class II |
About this recall
Is Apollo Care Semaglutide 12.5MG recalled?
Yes. Apollo Care, LLC recalled it on July 29, 2026; FDA published it August 19, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Presence of Particulate Matter; identified as a nylon/polyamide and silk/proteinaceous-type material
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.