FDAFDA · Food and drugs·Recall number D-686-2013
Gentamicin Sulfate Injection USP 80 mg/2 mL(40 mg/mL as Gentamicin), 2 mL Single-dose Fliptop Vial, (NDC 0409-1207-13), Rx only, Manufactured by Hospira, Inc, Lake Forest, IL 60046 USA.
Published July 17, 2013 · Recall initiated: May 2, 2013
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: visible particles were identified floating in the primary container.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- GENTAMICIN SULFATE
- Manufacturer
- Hospira Inc.
- Distributor
- Nationwide
- Lot
- Lot 07-067-DK Exp. 07/13
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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