Drug recall D-686-2013
Product
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.
Reason for recall
Presence of Particulate Matter: visible particles were identified floating in the primary container.
Lots and codes
Lot 07-067-DK Exp. 07/13
Recall details
- Recalling firm
- Hospira Inc., Lake Forest, IL
- Quantity
- 168,300 vals
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- May 2, 2013
- Terminated
- October 28, 2014
Related products
- Gentamicin Sulfate – drug information
- NDC 0409-1207 Gentamicin Sulfate · Gentamicin Sulfate 40 mg/mL · Hospira, Inc.