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K. C. Pharmaceuticals, Inc.

Country not established FDA establishment FEI 2026940

Devices
0
Registrations
FDA
FDA recalls
7

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
2026940
Address
3220 PRODUCER WAY, POMONA, CA, 91768

FDA recalls7

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

  • 2010

    • 3 Feb 2010 Z-1222-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005
    • 3 Feb 2010 Z-1223-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005
    • 3 Feb 2010 Z-1224-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005
    • 3 Feb 2010 Z-1225-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005
    • 3 Feb 2010 Z-1226-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005
    • 3 Feb 2010 Z-1227-2010 Unclassified (pre-2012) Terminated The recall was initiated because the affected lots were manufactured between two failed media fills; therefore the lots produced cannot be assured as being free of contamination and may not be sterile. Distribution: Nationwide Distribution. Submission number: P930005

  • 2004

    • 4 Oct 2004 Z-0060-05 Unclassified (pre-2012) Terminated Routine testing indicates product does not meet the expiration date in all cases. Distribution: Nationwide

This is an FDA establishment record without devices in deviCERTS.