FDAFDA · Food and drugs·Recall number Z-1824-2012
HEPARIN LOCK FLUSH SOLUTION, USP, 10 USP Units/mL, 1 mL Multiple Dose Vial, plastic vial, vial size 3 mL, NDC 63323-544-01, Product Code 504401, Rx only To maintain patency of an indwelling venipuncture device designed for intermittent injection or infusion therapy or blood sampling.
Published June 27, 2012 · Recall initiated: May 20, 2010
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
CGMP Deviations: Incomplete documentation associated with test results.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- App Pharmaceuticals Llc
- Distributor
- Nationwide Distribution and Puerto Rico
- Lot
- Lot 406952 (Expiration Date 02/11)
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.