CLASS II ONGOING Drug recall · Reported 19 Aug 2026 · FDA Enforcement Report

Semaglutide 5mg (1mg/mL), Glycine 25 mg recalled by Apollo Care

Apollo Care is recalling Semaglutide 5mg (1mg/mL), Glycine 25 mg (5mg/mL) Sterile Multi-Dose Vial, distributed nationwide in the US. The recall was initiated on 29 Jul 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot: AC-017272, Exp. 12/12/2026.
Quantity recalled250 vials.

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0754-2026
FDA event ID
99505
Recalling firm
Apollo Care, Columbia, MO
Classification
Class II
Status
Ongoing
Recall initiated
29 Jul 2026
FDA classified
7 Aug 2026
Reported
19 Aug 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Particulate Matter

Timeline

29 Jul 2026Recall initiated by company
7 Aug 2026Classified by FDA+9 days
19 Aug 2026Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

Nationwide within the U.S

Nationwide

Questions about this recall

Is Semaglutide 5mg (1mg/mL), Glycine 25 mg (5mg/mL) Sterile Multi-Dose Vial recalled?

Yes. Apollo Care recalled Semaglutide 5mg (1mg/mL), Glycine 25 mg (5mg/mL) Sterile Multi-Dose Vial on 29 Jul 2026. The recall is Class II and its status is Ongoing. Recall number D-0754-2026.

Why was it recalled?

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

Which lots are affected?

Lot: AC-017272, Exp. 12/12/2026.

Where was it sold?

Nationwide within the U.S

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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