FDAFDA · Food and drugs·Recall number D-0574-2018
Levofloxacin in 5% Dextrose Injection, 250 mg/50 mL (5 mg/mL), 50 mL Single-Use flexible container, Rx Only, Manufactured for: AuroMedics Pharma LLC 6 Wheeling Drive, Dayton, NJ 08810 Manufactured for: Aurobindo Pharma Limited IDA, Pashamylaram - 502307, India ---- NDC 55150-243-46
Published March 7, 2018 · Recall initiated: January 12, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Particulate Matter; contains visible particulate matter identified as mold.
What to do
Voluntary: Firm initiated · Press Release
Recall details
- Brand
- LEVOFLOXACIN
- Manufacturer
- AuroMedics Pharma LLC
- Distributor
- Nationwide
- UPC
- 0355150244478
- Lot
- Lot CLF160003, exp May 2018
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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