FDA Device recall Z-1232-2015
Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials
- FDA Device
- Class II
- terminated
- Published 2015-03-11
On 2015-03-11 the FDA classified a Class II recall of Oxoid Legionella BCYE Growth Supplement SR0110A packaged in packs of 10- 100 ml vials by Remel, citing use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1232-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-02-05 |
| Published | 2015-03-11 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Remel |
| Distribution | MI, ND, SC, TN, TX |
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
Use of the product may not provide adequate recovery and could result in false negative identification of Legionella pneumophila.
Identifiers
| code_info | Lot No. 1545171 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1232-2015%22
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