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Recall Observatory FDA recall evidence

Drug product

Pentreotide (10 uGm), Not for Direct Injection, Synthetopes, Inc.

D-1399-2019

May 28, 2019

Class II

Product summary

Firm
Synthetopes Inc
Event
Event 82969
Status
Terminated
Classification
Class II
Quantity
20 vials
Official record key
drug-enforcement:D-1399-2019

Official wording

Reason: Lack of Processing Controls.

Code information: All lots remaining within expiry.

Distribution pattern: Nationwide.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    Lack of Processing Controls