Integrity Biochem HSC70-LV
CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.
Departures from current Good Manufacturing Practice found in production or during FDA inspection. A broad quality-system cause: the batch was made under conditions that fall short of FDA manufacturing standards.
1,754 FDA drug recalls with this cause, newest first.
This category covers departures from current Good Manufacturing Practice during production. It is FDA's broadest label, used when a facility's own process control failed somewhere along the line even if no single ingredient was proven unsafe on its own. Where the report names a specific consequence - a temperature excursion, a contaminant, a potency problem - we file the recall under that more specific cause instead; what remains here is the genuinely general case.
CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.
CGMP Deviation: Third party test results showing a presence of acetal and acetaldehyde at levels above USP specified amounts.
Incorrect Product Formulation: Hydrophilic Colloidal Silica was used to manufacture the product rather than Hydrophobic Colloidal Silica as required by the manufacturing process.
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations: Products not manufactured under current good manufacturing practices.
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
CGMP Deviations
cGMP deviations: Batch was released prior to approval.
cGMP deviations: Batch was released prior to approval.
CGMP deviation: product released prior to supplier approval.
cGMP deviations: due to shipment of rejected units.
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
CGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
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