Batch recall — LARMES ARTIFICIELLES MARTINET 5.6 mg/0.4 ml (batches 2X25 and 2X26)
Teofarma, in agreement with the ANSM, is recalling batches 2X25 and 2X26 of LARMES ARTIFICIELLES MARTINET (single-dose eye drops) due to a potential risk of microbial contamination. Instructions for community pharmacies, wholesalers and hospital pharmacies.
Alert reference
Alert No. MED26-A014-B014 — 30 April 2026
TEOFARMA, in agreement with the ANSM and as a precaution, is recalling the batches below due to a potential risk of microbial contamination identified during revalidation of the production line.
At the time of this notice, no adverse effects or quality complaints had been reported.
Affected product
- LARMES ARTIFICIELLES MARTINET 5.6 mg/0.4 ml — eye drops, solution
- Pack: 20 single-dose containers
- CIP code: 3400936908154
Recalled batches
- Batch 2X25 — expiry 05/2028
- Batch 2X26 — expiry 05/2028
Immediate action required
- Quarantine all stock from batches 2X25 and 2X26 and stop dispensing it.
- Community pharmacies: return the product to your usual wholesaler, regardless of the original purchasing channel.
- Wholesalers & hospital pharmacies: return to Movianto — CSP, 76-78 avenue Du Midi, 63800 Cournon-d'Auvergne.
Arrange a return with Pharmafit Provence
Our team supports pharmacies in the region with returns and credits for the affected batches. Contact us at provence@pharmafit.fr or on 06 84 62 94 47.
Manufacturer contact
Teofarma Srl — Viale Certosa 8/A, 27100 Pavia (Italy) Phone: +39 (0)382 422 008 Email: servizioclienti@teofarma.it
Recall level
Community pharmacies, healthcare establishments and the pharmaceutical distribution network. Issuer: TEOFARMA. Contact: Paolo Badini.
