Remel Europe recalls

2 official recalls and safety alerts involving Remel Europe since 2026-04, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Remel Europe or the relevant agency.

1. 2026-08-19
2. US
   Drugs & medicalClass II

   Remel Europe Ltd. recalls Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics

   Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.

   FDA · DeviceRemel Europe Ltd.US Nationwide distribution.Official notice →
3. 2026-04-29
4. US
   Drugs & medicalClass II

   Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301

   Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds. Cross-reactivity may result in the misidentification of a Salmonella 9-O serotype as a 2-O serotype.

   FDA · DeviceRemel Europe Ltd.Worldwide - US Nationwide distribution to the states of AL, CA, FL, IA, IL,…Official notice →