Reported Sep 11, 2024 · Ongoing

Semaglutide / Cyanocobalamin Injection: 2.5/0.5 mg/mL, 2 mL Multiple Dose Vial, Compounded Rx Product, ProRX…

ProRx LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: ProRx LLC · 619 Jeffers Cir · Exton, PA · 19341-2540

Is this the product you have?

  • Semaglutide / Cyanocobalamin Injection
    • 2.5/0.5 mg/mL
    • 2 mL Multiple Dose Vial
    • Compounded Rx Product
    • ProRX 267-565-7008
    • NDC 84139-225-02
Lot codes and dates
    • Lot # ProRx031924-1
    • BUD 09/18/2024
Amount recalled
500 vials

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

Lack of Assurance of Sterility

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new ProRx LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 7:55 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.