Class I · Most seriousActive recall
Dextrose Injection
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberLot #: Y495066, Exp. Date July 31, 2027
Where it was soldU.S. Nationwide.
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
Presence of Particulate Matter: particulate matter identified as stainless steel particles in the solution.
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 byMade in USA
| Distributed by / for | Baxter Healthcare Corporation |
| NDC | 00338-0719-06 |
Show the full FDA record
| Full product label | Dextrose Injection, USP, 70 %, 2000 mL bags, Rx Only, Baxter Healthcare Corporation Deerfield, IL, 60016, Made in USA, NDC 00338-0719-06 |
| Recalling firm | Baxter Healthcare Corporation |
| Distribution | U.S. Nationwide. |
| Quantity | 606 bags |
| Recall initiated | 2026-08-17 |
| Report date | 2026-09-16 |
| Recall completed | — |
| Recall number | D-0850-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Deerfield IL 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.