FDAFDA · Food and drugs·Recall number D-1222-2019
Lidocaine 1% - Sodium Bicarb 8.4% 10:1, 10 mL syringe, For Intradermal Use Only, Made by: Enterprise Pharmacy, 4400 Golf Acres Drive, Bldg. J Suite E, Charlotte, NC, 28208.
Published May 1, 2019 · Recall initiated: April 12, 2019
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
Lack of sterility assurance.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CMC Enterprise Pharmacy
- Distributor
- NC
- Lot
- Lots: ED051902 Exp. 4/14/2019; ED101902 Exp. 4/19/2019
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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