Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of… — Class II medical device recall Z-1232-2015
Terminated recall by Remel Inc, reported 2015-03-11, distributed in MI, ND, SC, TN, TX. Use of the product may not provide adequate recovery and could result in false negative identification of Legi
| Recall number | Z-1232-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2015-02-05 |
| Classified | 2015-03-02 |
| Reported by FDA | 2015-03-11 |
| Terminated | 2017-02-13 |
| Distributed | MI, ND, SC, TN, TX |
| Quantity | 24 packages |
| Lot numbers | 1545171 |
Product
Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England and Oxoid Ltd., Basingstoke, Hants, England.
Reason for recall
Use of the product may not provide adequate recovery and could 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-1232-2015. 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.