FDAFDA · Food and drugs·Recall number D-0138-2020
Sodium Chloride Injection USP 0.9%, packaged in 1 - 125 mL Ultraject Prefilled Syringe For Power Injection per carton, RFID Technology, Rx Only, Manufactured by: Liebel-Flarshelm Company, LLC., Raleigh, NC 27616; NDC 0019-1188-27.
Published October 16, 2019 · Recall initiated: September 13, 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
Labeling: Not Elsewhere Classified: RFID formatting error which reads product in Ultraject syringe as expired and will not allow injection of product by the Optivantage injector.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- SODIUM CHLORIDE
- Manufacturer
- GUERBET LLC
- Distributor
- Nationwide in the USA
- UPC
- 0300191188816
- Lot
- Lots: L159A, Exp. 06/2021; L169A, Exp. 07/2021
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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