Skip to content
Recall Observatory FDA recall evidence

Drug product

Carvediol Tablets, USP, 6.25 mg, 100-count bottle (NDC 57664-244-18), 500-count bottle (NDC 57664-244-13), 1000-count bottle (NDC 57664-244-18), Rx Only, Manufactured by: ALKALOIDA Chemical Company Zrt 440 Tisavasvari Kabay Janos u. 29 Hungary, Distributed by Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512

D-1505-2016

June 27, 2016

Class III

Product summary

Firm
Sun Pharmaceutical Industries, Inc.
Event
Event 74694
Status
Terminated
Classification
Class III
Quantity
2,952 HDPE bottles
Official record key
drug-enforcement:D-1505-2016

Official wording

Reason: Failed Impurities/Degradation Specifications

Code information: Lot #: AVF0254/C, AVF0254/B, AVF0254/C; Exp. 02/17

Distribution pattern: Nationwide

Derived failure modes

  • Potency or specification failure

    reason.potency_specification_failure · v1.0.0

    Failed Impurities/Degradation Specifications