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FDA Recalls

In the News

News
05/14/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) issued a Class II recall on duloxetine delayed-release capsules due to deviations in Current Good Manufacturing Practice (CGMP) regulations.
The US Food and Drug Administration (FDA) issued a Class II recall on duloxetine delayed-release capsules due to deviations in Current Good Manufacturing Practice (CGMP) regulations.
The US Food and Drug...
05/14/2026
Pharmacy Learning Network
News
05/14/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall on enalapril maleate tablets for failed impurities/degradation specifications.
The US Food and Drug Administration (FDA) has issued a Class II recall on enalapril maleate tablets for failed impurities/degradation specifications.
The US Food and Drug...
05/14/2026
Pharmacy Learning Network
News
05/14/2026
Rebecca Amrick
The US Food and Drug Administration (FDA) has issued a Class II recall for naproxen oral suspension due to excessive amounts of lead and lithium.
The US Food and Drug Administration (FDA) has issued a Class II recall for naproxen oral suspension due to excessive amounts of lead and lithium.
The US Food and Drug...
05/14/2026
Pharmacy Learning Network
News
05/07/2026
Hannah Musick
The US Food and Drug Administration (FDA) has issued a Class II recall for Fresenius DELFLEX peritoneal dialysis solutions due to potential bag leaks compromising sterility, affecting more than 80 000 units used in renal care.
The US Food and Drug Administration (FDA) has issued a Class II recall for Fresenius DELFLEX peritoneal dialysis solutions due to potential bag leaks compromising sterility, affecting more than 80 000 units used in renal care.
The US Food and Drug...
05/07/2026
Pharmacy Learning Network
News
05/07/2026
Hannah Musick
A class II recall has been issued for FRESHKOTE Lubricant Eye Drops due to sterility assurance concerns, affecting more than 50 000 units used for dry eye relief.
A class II recall has been issued for FRESHKOTE Lubricant Eye Drops due to sterility assurance concerns, affecting more than 50 000 units used for dry eye relief.
A class II recall has been...
05/07/2026
Pharmacy Learning Network