FDA recall, , Moderate risk
Apollo Care Semaglutide Injection Vials
Semaglutide sterile multi-dose vials contain particulate matter identified as nylon/polyamide and silk/proteinaceous-type material.
Summary by Recall Canary from the FDA notice
What happened
Apollo Care, LLC of Columbia, Missouri recalled multiple Semaglutide sterile multi-dose vials because they contain particulate matter identified as nylon/polyamide and silk/proteinaceous-type material. The FDA listed the products in its Enforcement Report on August 7, 2026, and the recall began July 29, 2026. The products were distributed nationwide within the U.S.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Match your product and all the details in one listed combination.
An NDC (National Drug Code) is usually printed on the drug's label.
Semaglutide
- Strength
- 7.5 mg
- NDC
- 71170-721-01
- Lot code
- AC-017273
- Strength
- 12.5 mg
- NDC
- 71170-495-05
- Lot code
- AC-017108
- Strength
- 2.5 mg
- NDC
- 71170-711-02
- Lot code
- AC-017271
- Strength
- 2.25 mg
- NDC
- 71170-811-02
- Lot code
- AC-017114
- Strength
- 0.9 mg
- NDC
- 71170-810-01
- Lot code
- AC-017131
- Strength
- 6.75 mg
- NDC
- 71170-821-01
- Lot code
- C-017115
- Strength
- 9 mg
- NDC
- 71170-822-02
- Lot code
- AC-017125
- Strength
- 10 mg
- NDC
- 71170-722-02
- Lot code
- AC-017274
- Strength
- 20 mg
- NDC
- 71170-724-04
- Lot code
- AC-017275
- Strength
- 4.5 mg
- NDC
- 71170-812-03
- Lot code
- AC-017124
- Strength
- 5 mg
- NDC
- 71170-712-03
- Lot code
- AC-017272
Recall details
- Company began the recall
- Sold in
Nationwide within the U.S
- Company
- Apollo Care, LLCColumbia, Missouri
- Hazard
- Foreign object
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99505
- Recall numbers
- D-0747-2026 to D-0757-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
