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Recall Observatory FDA recall evidence

Drug product

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.

D-0138-2020

September 13, 2019

Class III

Product summary

Firm
GUERBET LLC
Event
Event 83798
Status
Terminated
Classification
Class III
Quantity
3140 syringes
Official record key
drug-enforcement:D-0138-2020

Official wording

Reason: 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.

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

Distribution pattern: Nationwide in the USA

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.