CLASS II ONGOING Drug recall · Reported 26 Apr 2023 · FDA Enforcement Report

C-Semaglutide 5mg/mL injection vials recalled by Pharmacy Plus

Pharmacy Plus is recalling C-Semaglutide 5mg/mL injection vials, distributed in Mississippi. The recall was initiated on 13 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 73810, Exp. Date 5/1/2023
Quantity recalled45 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-0538-2023
FDA event ID
92121
Recalling firm
Pharmacy Plus, Hattiesburg, MS
Classification
Class II
Status
Ongoing
Recall initiated
13 Apr 2023
FDA classified
19 Apr 2023
Reported
26 Apr 2023
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Sterility

Timeline

13 Apr 2023Recall initiated by company
19 Apr 2023Classified by FDA+6 days
26 Apr 2023Published in enforcement report+7 days

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

Reason for recall

Lack of assurance of sterility.

A sterility recall means a product that must be sterile, such as an injection or eye drop, may be contaminated. Using a non-sterile product can cause serious infection.

Product as listed by the FDA

C-Semaglutide 5mg/mL injection, 0.5mL vials, Rx only, Vital Care Compounder 115 South 40th Ave, Suite A Hattiesburg, MS 39402

Where it was distributed

MS only

Mississippi

Questions about this recall

Is C-Semaglutide 5mg/mL injection vials recalled?

Yes. Pharmacy Plus recalled C-Semaglutide 5mg/mL injection vials on 13 Apr 2023. The recall is Class II and its status is Ongoing. Recall number D-0538-2023.

Why was it recalled?

Lack of assurance of sterility.

Which lots are affected?

Lot #: 73810, Exp. Date 5/1/2023

Where was it sold?

MS only

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.

More recalls from Pharmacy Plus

All 54