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Medicine recalls and shortages › Recalls and defects › 25 Nov 2025
Medicines recall

Moclobemide 150mg tablets

Issued on 25 Nov 2025 · source: MHRA — Medicines and Healthcare products Regulatory Agency
Affected batches: I3602 (30/09/2027), H4610 (31/05/2029)
Check the batch number on the pack. The medicine remains licensed; other batches are not affected.
Class 4 defect notification · DMRC - 37693641 · licence holder: Lexon UK Ltd · active ingredient: Moclobemide

What this means

The MHRA has issued a medicines recall or defect notification. Class 1: risk to life, immediate recall. Class 2: may cause mistreatment or harm, recall within 48 hours. Class 3: unlikely to cause harm, recall within 5 days. Class 4 (defect notification): no recall, caution in use. The medicine remains licensed; only the listed batches are affected. Do not stop treatment without speaking to your doctor or pharmacist.

Class 4 defect notification · DMRC - 37693641

ProductLicenceActive ingredientGTIN
Moclobemide 150mg tabletsMoclobemide05037015030871

Batches (expiry): I3602 (30/09/2027), H4610 (31/05/2029)

Background: Lexon UK Ltd has informed the MHRA that the Patient Information Leaflet (PIL) in the cartons for the batches listed in this notification is missing important updated safety information. Lexon UK Ltd has confirmed that 326 packs of the affected batches are already distributed in the market. The missing information from the PIL is detailed in this notification: 2. What you need to know before you take Moclobemide

Tracked from information published by the MHRA and the NHSBSA. This information is for guidance only and does not replace advice from your doctor or pharmacist.