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Recall Observatory FDA recall evidence

Drug product

Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-402-05.

D-0890-2018

June 08, 2018

Class II

Product summary

Firm
Ingenus Pharmaceuticals Llc
Event
Event 80254
Status
Terminated
Classification
Class II
Quantity
34964 vials
Official record key
drug-enforcement:D-0890-2018

Official wording

Reason: Superpotent Drug: High out of specification assay value results for potency.

Code information: Lot #: 17034-1, 17035-1, 17036-1; Exp. 08/19

Distribution pattern: Nationwide in the USA

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Superpotent