Class II · ModerateRecall completed
Albuterol 0.083% Inh Sol. 30 days supply
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberAll lots remaining within expiry dispensed 12/01/2017 through 02/12/2018
Where it was soldMS, LA, AR, IL, FL
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
Lack of Processing Controls.
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 | Kroger Specialty Pharmacy, Inc. |
| NDC | 76204-0200-60 |
Show the full FDA record
| Full product label | Albuterol 0.083% Inh Sol. 30 days supply, Rx Only, 39183, NDC 76204-0200-60, 30 |
| Recalling firm | Kroger Specialty Pharmacy, Inc. |
| Distribution | MS, LA, AR, IL, FL |
| Quantity | Unknown |
| Recall initiated | 2018-04-03 |
| Report date | 2018-05-16 |
| Recall completed | 2020-05-07 |
| Recall number | D-0735-2018 |
| Classification | Class II |
| FDA status | Terminated |
| Origin on file | Vicksburg MS 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.