Remel Europe recall: Thermo Fisher Diagnostics Neisseria meningitidis Gp C
Remel Europe Ltd. is recalling Thermo Fisher Diagnostics Neisseria meningitidis Gp C – 26 units. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on July 17, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Thermo Fisher Diagnostics Neisseria meningitidis Gp C |
| Brand | Remel Europe |
| Company | Remel Europe Ltd. |
| Type | Medical devices |
| Classification | Class II |
| Recall date | July 17, 2026 |
| Published by FDA | August 19, 2026 |
| Quantity | 26 units |
| Recall ID | 99450 |
Recalled products
- Thermo Fisher Diagnostics Neisseria meningitidis Gp C 2ml/VL, Product Number R30166901; invitro diagnostics
- FDA recall number
- Z-2927-2026
- Codes, lots and dates
- UDI/DI 05056080501161, Lot Numbers: 6214791, exp. 18/03/2025; 6175327, exp. 04/12/2027; 6148809, exp. 30/09/2027; 6002010, exp. 31/07/2027.
- Quantity
- 26 units
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99450
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Dartford, United Kingdom
Why it was recalled
The reason the FDA lists: “Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.”
Where it was sold
Nationwide. Distribution as the FDA records it: “US Nationwide distribution.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99450, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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About this recall
Is Remel Europe Thermo Fisher Diagnostics Neisseria meningitidis Gp C recalled?
Yes. Remel Europe Ltd. recalled it on July 17, 2026; FDA published it August 19, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Certain lots of Neisseria meningitidis Gp C 2ml/VL, R30166901, are not performing to IFU criteria not positive to ATCC13102 within 60 Seconds.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.