Oxoid Legionella BCYE Growth Supplement SR0110A — Class II medical device recall Z-0200-2015
Terminated recall by Remel Inc, reported 2014-11-19, distributed in ND, TX, VT. Recalled product may not provide adequate recovery of Legionella pneumophila when used as directed and may res
| Recall number | Z-0200-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2014-10-17 |
| Classified | 2014-11-10 |
| Reported by FDA | 2014-11-19 |
| Terminated | 2017-02-13 |
| Distributed | ND, TX, VT |
| Lot numbers | 1451506 |
| Expiration dates | 2016-02-26 |
Product
Oxoid Legionella BCYE Growth Supplement SR0110A, packaged in 100 ml vials, 10/pkg. A growth supplement for the isolation of Legionella.
Reason for recall
Recalled product may not provide adequate recovery of Legionella pneumophila when used as directed and may result in false negative identification of Legionella pneumophila.
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-0200-2015. 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.