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Recall Observatory FDA recall evidence

Drug product

15 units Oxytocin added to 0.9% Sodium Chloride Injection, 250 mL Viaflex Bag, Rx only, PharMEDium Serivces, LLC

D-0422-2018

February 05, 2018

Class II

Product summary

Firm
PharMEDium Services, LLC
Event
Event 79063
Status
Terminated
Classification
Class II
Quantity
24 Viaflex Bag
Official record key
drug-enforcement:D-0422-2018

Official wording

Reason: Lack of assurance of sterility: Three lots were released where there was a failure to follow proper testing and investigation procedures. Product may be out of specification (OOS) for endotoxin.

Code information: Lot #: 180040003D, Exp 3/18/18

Distribution pattern: Product was distributed to SC, FL, NY, NY,WA

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    out of specification
  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    Lack of assurance of sterility