FDARecall 99824Medicines
What to do
The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Talk to your pharmacist or doctor before stopping a medicine.Note from Recalls Watch, not agency text.
Read the official notice on accessdata.fda.gov (opens in a new tab)
Hazard
Why it was recalled
Lack of Assurance of Sterility
FDA classification: Class II. Use may cause temporary or medically reversible health consequences, or the chance of serious consequences is remote. Status: Ongoing.
Is it yours? Products and codes
Dopamine HCl Inj., USP, 200 mg/5 mL (40 mg/mL), 5 mL Single-dose, 25 vials per tray, Rx only, Distributed by Hospira, Inc., Lake Forest, IL 60045 USA, Vial NDC 0409-5820-11, Carton NDC 0409-5820-01.
- Lot or code
- Lot # NL5230, Exp Date:10/2027
- FDA recall number
- D-0853-2026
Distribution (FDA): US Nationwide.
About this record
- Issued by
- U.S. Food and Drug Administration
- Firm
- Pfizer
- Title
- Composed by Recalls Watch from fields of the record; FDA records have no title.