FDA Device recall Z-0808-2013
Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box
- FDA Device
- Class II
- terminated
- Published 2013-02-20
On 2013-02-20 the FDA classified a Class II recall of Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box by Remel, citing the firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0808-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-08-21 |
| Published | 2013-02-20 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Remel |
| Distribution | US |
Product
Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK.
Reason
The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.
Identifiers
| code_info | Lot 1186069 |
|---|
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-0808-2013%22
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