Class III · Lower riskRecall completed
Ceftriaxone Sodium
Unlikely to cause harm — often a labeling or packaging issue.
Does this affect you?
Check your lot numberSandoz - Lot GJ7151(Pfizer- Lot 670028M); Exp. 07/19
Where it was soldWI
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Labeling: Missing Label
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
Made bySandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria
| Brand name | CEFTRIAXONE SODIUM |
| Generic name | CEFTRIAXONE SODIUM |
| Active ingredient(s) | CEFTRIAXONE SODIUM |
| Distributed by / for | Sandoz Inc |
| NDC | 0409-7332-01 |
Show the full FDA record
| Full product label | Ceftriaxone for Injection, USP, 1 gram, 10 Single use Vials, Rx only, For IM or I.V. Use, Manufactured by: Sandoz GMbH for Hospira Worldwide, Inc., Lake Forest, Il 60045, USA, Made in Austria, NDC 0409-7332-01 |
| Recalling firm | Sandoz Inc |
| Distribution | WI |
| Quantity | 139,430 vials |
| Recall initiated | 2016-10-19 |
| Report date | 2016-11-30 |
| Recall completed | 2017-07-27 |
| Recall number | D-0145-2017 |
| Classification | Class III |
| FDA status | Terminated |
| Origin on file | Princeton NJ United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.