PlainRecalls
FDA Drug Moderate Class II Terminated

Desoximetasone USP (Micronized) for prescription compounding, 5g, RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327, NDC 58597-8634-2.

Reported: February 28, 2018 Initiated: February 9, 2018 #D-0483-2018

Product Description

Desoximetasone USP (Micronized) for prescription compounding, 5g, RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327, NDC 58597-8634-2.

Reason for Recall

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Details

Units Affected
N/A
Distribution
Nationwide within USA.
Location
Waterford, MI

Frequently Asked Questions

What product was recalled?
Desoximetasone USP (Micronized) for prescription compounding, 5g, RX only, packed by American Pharmaceutical Ingredients, LLC 6650 Highland Road, Waterford, MI 48327, NDC 58597-8634-2.. Recalled by American Pharmaceutical Ingredients LLC. Units affected: N/A.
Why was this product recalled?
CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 28, 2018. Severity: Moderate. Recall number: D-0483-2018.