Oxoid Legionella Pneumo Groups 2-14 — Class II medical device recall Z-1474-2014
Terminated recall by Remel Inc, reported 2014-04-30, distributed in CA, FL, IL, MA, ME, NJ, PA, TN…. A reagent contained within the product may return false negative results.
| Recall number | Z-1474-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2014-03-17 |
| Classified | 2014-04-18 |
| Reported by FDA | 2014-04-30 |
| Terminated | 2014-12-11 |
| Distributed | CA, FL, IL, MA, ME, NJ, PA, TN, TX, VA, VT |
| Lot numbers | 1265362, 1265366, DR0802 |
| Expiration dates | 2014-06-30 |
Product
Oxoid Legionella Pneumo Groups 2-14, DR0802M, containing 50 tests per box. The box contains a variety of components, one of which is Oxoid L. pneumophila Group 2-14 Latex Reagent, DR0802. The responsible firm on the label is Oxoid Ltd., Basingstoke, Hants, England.
Reason for recall
A reagent contained within the product may return false negative results.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1474-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.