FDAFDA · Food and drugs·Recall number D-099-2013
Lidocaine HCl Injection, USP, 1% (10 mg/mL), 30 mL Single-dose Teartop Vial, packaged in 25-count vials per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045; NDC 0409-4279-02.
Published December 26, 2012 · Recall initiated: October 4, 2012
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: Report of a vial containing visible particulate matter embedded in the glass wall which has the potential to dislodge resulting in the presence of particulate matter in the product.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- LIDOCAINE HYDROCHLORIDE
- Manufacturer
- Hospira, Inc.
- Distributor
- Nationwide
- Lot
- Lot #: 14-277-DK*, Exp 02/01/14; * may be followed by 01
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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