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Recall Observatory FDA recall evidence

Drug product

Oxycodone Hydrochloride Oral Solution, USP 5 mg/5 mL, a). 5 mL, 50 unit dose cups of 5 mL per case (NDC No. 66689-401-50), b). 500 mL, 12 bottles per case (NDC No. 66689-403-16), Rx only, Manufactured by VistaPharm, Largo, FL 33771.

D-0464-2017

January 18, 2017

Class II

Product summary

Firm
VistaPharm, Inc.
Event
Event 75650
Status
Terminated
Classification
Class II
Quantity
42,776 unit dose cups and 17,403 bottles
Official record key
drug-enforcement:D-0464-2017

Official wording

Reason: CGMP Deviations: Purified water used to manufacture the drug products may have been contaminated with Burkholderia cepacia.

Code information: a). Lot No. 427900, 426700 (Exp. 11/17), 424800, 423600 (Exp. 10/17), 420800 (09/17), 416300 (08/17), 407700, 407300 (Exp. 06/17), 405900, 403900 (Exp. 05/17) b). Lot No. 426900 (Exp. 11/17), 404700 (Exp. 05/17), 390200 (Exp. 02/17)

Distribution pattern: Nationwide

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    CGMP Deviations
  • Microbial contamination

    reason.microbial_contamination · v1.0.0

    contaminated with Burkholderia cepacia