Has duloxetine been recalled?
I can’t confirm whether duloxetine is under an active or recent recall from the information provided here. Recalls are time- and brand-specific, and they depend on the exact product (brand name), dose strength, and manufacturer.
Which duloxetine product might be affected?
Duloxetine is sold under multiple brand and generic versions (for example, commonly as Cymbalta for certain markets), and recalls—when they happen—typically name:
- the specific manufacturer,
- the dosage strength (e.g., 20 mg, 30 mg, 60 mg),
- the formulation (capsule/tablet),
- and affected lot numbers/expiration dates.
To check accurately, you’d need the exact name on your bottle and any lot/expiration details.
How to check quickly (what to look for)
The most reliable way to verify whether your specific duloxetine is recalled is to:
- check the lot/expiration number printed on the packaging against recall notices, and
- search the drug name plus “recall” using official databases (such as your country’s FDA/medicines safety authority site).
What to do if your duloxetine is listed in a recall
If your lot number matches a recall notice, follow the instructions on that notice (often “stop use,” “return,” or “contact your pharmacy”). Don’t switch doses or stop abruptly without medical guidance, especially for antidepressants and serotonin-norepinephrine reuptake inhibitors.
Tell me your details and I’ll help you narrow it down
If you share:
1) the exact product name (brand/generic) on your bottle,
2) strength (mg), and
3) the lot number and expiration date (if available),
I can help you determine whether your specific duloxetine could be part of a recall and what the next step should be.
Sources: None provided in the question.