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Semaglutide 12.5mg Multi-Dose Vial
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DRUG RECALLMODERATE

Semaglutide 12.5mg Multi-Dose Vial

Apollo Care recalls semaglutide 12.5mg vials due to particulate matter.

What to do

Stop using the recalled semaglutide vials immediately and contact your healthcare provider for guidance. Return the product to the place of purchase or follow the firm's instructions for disposal.

Recalled
Listed
Updated
Recall No.
D-0755-2026
Agency
FDA
Firm
Apollo Care, LLC
Recall ID
99505
Status
ONGOING

Why it was recalled

Apollo Care is recalling semaglutide 12.5mg (2.5mg/mL) 5 mL sterile multi-dose vials due to the presence of particulate matter identified as nylon/polyamide and silk/proteinaceous-type material. Use of the affected product may pose a risk of adverse reactions.

Is mine affected?

This recall covers 11 products. Check the NDC or UPC and strength printed on the package. Yours is affected if it matches one below.

SEMAGLUTIDE

Lot codeStrengthNDC / UPCRecall #
AC-017273, 20267.5 mgNDC 71170-721-01D-0755-2026
AC-017108, 202612.5 mgNDC 71170-495-05D-0747-2026
AC-017271, 20262.5 mgNDC 71170-711-02D-0753-2026
AC-017114, 20262.25 mgNDC 71170-811-02D-0748-2026
AC-017131, 20260.9 mgNDC 71170-810-01D-0752-2026
C-017115, 20266.75 mgNDC 71170-821-01D-0749-2026
AC-017125, 20269 mgNDC 71170-822-02D-0751-2026
AC-017274, 202610 mgNDC 71170-722-02D-0756-2026
Show all 11 products
Lot codeStrengthNDC / UPCRecall #
AC-017275, 202620 mgNDC 71170-724-04D-0757-2026
AC-017124, 20264.5 mgNDC 71170-812-03D-0750-2026
AC-017272, 20265 mgNDC 71170-712-03D-0754-2026

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Other Foreign Material recalls

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification