Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Lack of Processing Controls.
What was recalled
Pulmicort Respules 0.5 mg/2mL s, 30 days supply, NDC 00186-1989-04
- Recalling firm
- Kroger Specialty Pharmacy, Inc.
- NDC code
- 00186-1989-04
- Origin
- MS, United States
- Initiated by
- Voluntary: Firm initiated
- FDA recall number
- D-0739-2018
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.
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