Remel Europe Ltd. recalls
Every recall we track for Remel Europe Ltd. — 3 in all, from 2020–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
3 recalls since 2017.
All FDA recall records for Remel Europe Ltd. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 2 | 0 | 2 |
What to do if you have a recalled Remel Europe Ltd. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Remel Europe Ltd. recalls
3 shown- Lower riskMedical device
Remel Europe Ltd. recalls Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics
Thermo Fisher Diagnostics recalls Neisseria meningitidis Gp C 2ml/VL test kits with Product Number R30166901 that may not detect bacteria within 60 seconds. Affected lots have specific expiration dates.
RemelJul 17, 2026 - Lower riskMedical device
Remel Europe Ltd. recalls Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Remel recalls Oxoid Agglutinating Sera (Salmonella 9-0 R30957301) due to cross-reaction with 2-0 serotypes. Affected lots may misidentify Salmonella 9-O as 2-O, risking incorrect identification in lab tests.
RemelMar 25, 2026 - Lower riskMedical device
Remel Europe Ltd. recalls Thermo Scientific Remel Bordetella pertussis Agglutinating Serum Product Number: R30165501, UDI-DI: 05056080501826 -
Remel recalls Bordetella pertussis agglutinating serum (R30165501) due to potential false negatives for serotypes 1 and 3 in tests. Affected units have specific product numbers and lot numbers.
RemelJul 23, 2020
Remel Europe Ltd. recall questions
How many recalls has Remel Europe Ltd. had?
3 recalls from Remel Europe Ltd. are on record with U.S. safety agencies, from 2020–2026.
What is the most recent Remel Europe Ltd. recall?
Remel Europe Ltd. recalls Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics, dated Jul 17, 2026. Every Remel Europe Ltd. recall is listed on this page, newest first.
What should I do if I have a recalled Remel Europe Ltd. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Remel Europe Ltd. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.