Duloxetine Cap recalls

The FDA has published 1 recall involving Duloxetine Cap since 2024. The latest was reported on 29 May 2024. Most were for nitrosamine impurity. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2024

Last 12 months0reported

Class I00% of total

Ongoing1latest 29 May 2024

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 0 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why duloxetine cap is recalled

Nitrosamine Impurity1100%

Companies

Preferred Pharmaceuticals1100%

By year

20241100%

Ongoing duloxetine cap recalls

1 active

Reported	Class	Recall	Company	Reason	Where
29 May 2024Drug	CLASS II	Duloxetine Delayed-Release Cap USP 30mg recalled	Preferred Pharmaceuticals	Nitrosamine Impurity	5 states

All duloxetine cap recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
29 May 2024Drug	CLASS II	Duloxetine Delayed-Release Cap USP 30mg recalled	Preferred Pharmaceuticals	Nitrosamine Impurity	5 states

Should you stop taking Duloxetine Cap?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.