RecallDepth
Class III Terminated

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.

Company
Guerbet Llc
Recall Initiated
September 13, 2019
Posted
October 16, 2019
Recall Number
D-0138-2020
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
3140 syringes
Firm Location
Princeton, NJ, United States

Reason for Recall

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.

Distribution

Nationwide in the USA

Lot / Code Info

Lots: L159A, Exp. 06/2021; L169A, Exp. 07/2021

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