Class II · ModerateRecall completed
Cyanocobalamin Injection
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot #: L200253, L200281, L200301, Exp 07/31/2024
Where it was soldTN
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: glass
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
| Distributed by / for | Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India |
| NDC | 16714-165-01 |
Show the full FDA record
| Full product label | Cyanocobalamin Injection, USP, 1,000mcg/mL, 1 mL Multiple-Dose Vial, Rx Only, Manufactured for: Northstar Rx LLC, Memphis, TN, 38141, Mfd. in India, NDC 16714-165-01. |
| Recalling firm | Zydus Pharmaceuticals (USA) Inc |
| Distribution | TN |
| Quantity | 432250 vials |
| Recall initiated | 2024-06-27 |
| Report date | 2024-07-24 |
| Recall completed | 2025-09-04 |
| Recall number | D-0600-2024 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Pennington 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.