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

Kimmtrak 200 micrograms/mL concentrate for solution for infusion

Issued on 25 Jun 2025 · source: MHRA — Medicines and Healthcare products Regulatory Agency
Affected batches: 3D009AA17 (31/03/2026), 3D009AA19 (31/03/2026), 3D009AA36 (31/03/2026)
Check the batch number on the pack. The medicine remains licensed; other batches are not affected.
Class 3 recall · DMRC-35860567 · PLGB: 36781/0001 · licence holder: Immunocore Limited · active ingredient: tebentafusp · licence PLGB: 36781/0001

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 3 recall · DMRC-35860567

ProductLicenceActive ingredientGTIN
Kimmtrak 200 micrograms/mL concentrate for solution for infusionPLGB: 36781/0001tebentafusp05056416800029

Batches (expiry): 3D009AA17 (31/03/2026), 3D009AA19 (31/03/2026), 3D009AA36 (31/03/2026)

Background: Immunocore Limited is recalling the batches listed above as a precautionary measure. The recall is due to a decrease in potency identified during stability testing. All other stability test results remain within specification. Only the batches listed in the above table are impacted. This does not affect other batches that are available. Advice for Healthcare Professionals:

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.