FDAFDA · Food and drugs·Recall number D-200-2013
CALCIUM GLUCONATE INJECTION, USP, 10% (100 mg/mL), 10 mL, Single Dose Vial, Rx only, For Direct Slow IV or IV Additive Use Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173 --- Product Code 31110, NDC 63323-311-10
Published March 20, 2013 · Recall initiated: February 1, 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
Labeling: Missing label
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Fresenius Kabi USA LLC (FK USA)
- Distributor
- Nationwide
- Lot
- Lot 6004889, Expiration Date 10/2014
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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