Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml… — Class II medical device recall Z-0578-2015
Terminated recall by Remel Inc, reported 2014-12-17, distributed nationwide. Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false n
| Recall number | Z-0578-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2014-11-13 |
| Classified | 2014-12-10 |
| Reported by FDA | 2014-12-17 |
| Terminated | 2015-01-29 |
| Distributed | Nationwide (US) |
| Lot numbers | 1374439 |
| Expiration dates | 2015-08-31 |
Product
Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials. A growth supplement for the isolation of Legionella.
Reason for recall
Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.
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-0578-2015. 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.