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Recall Observatory FDA recall evidence

Drug product

Provocholine pre-diluted in 0.9% Sodium Chloride Set II syringes, 0.0625mg/mL,3 mL; 0.25 mg/mL 3mL; 1 mg/mL 3mL; 4 mg/mL 3mL; 16 mg/ml 3mL, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC 45183-0674-80

D-1290-2016

April 20, 2016

Class II

Product summary

Firm
Pharmakon Pharmaceuticals, Inc.
Event
Event 73960
Status
Terminated
Classification
Class II
Quantity
142
Official record key
drug-enforcement:D-1290-2016

Official wording

Reason: Lack of Assurance of Sterility

Code information: All Sterile Compounded Products within Expiry

Distribution pattern: Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA

Derived failure modes

  • Sterility assurance

    reason.sterility_assurance · v1.0.0

    Lack of Assurance of Sterility