Class II · Moderate risk Terminated
Ceftriaxone for Injection
Reason Lack of Assurance of Sterility
Ceftriaxone
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of sterility assurance
What was recalled
CEFTRIAXONE (a) 1GM IN NS 50ML, (b)4GM IN NS 200ML, (c) 8GM IN NS 400ML, antibiotic, Rx only, used in a Curlin or Home pump, Sentara Home Infusion Pharmacy Services, 535 Independence Pkwy, Ste 300, Chesapeake, VA 23320,
- Recalling firm
- Sentara Infusion Services
- Origin
- VA, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0282-2023
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Other Ceftriaxone recalls
See all
Class II · Moderate risk Terminated
Ceftriaxone for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Ceftriaxone for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Ceftriaxone for Injection
Reason Lack of Assurance of Sterility
Class II · Moderate risk Terminated
Ceftriaxone for Injection
Reason Lack of Assurance of Sterility
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