Oxoid Antimicrobial Susceptibility Discs — Class II medical device recall Z-0808-2013
Terminated recall by Remel Inc, reported 2013-02-20, distributed nationwide. The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of a
| Recall number | Z-0808-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Remel Inc, Lenexa, KS, United States |
| Recall initiated | 2012-08-21 |
| Classified | 2013-02-12 |
| Reported by FDA | 2013-02-20 |
| Terminated | 2013-06-04 |
| Distributed | Nationwide (US) |
| Quantity | 23 units |
| Lot numbers | 1186069 |
| Model numbers | CT0119B |
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 for recall
The firm is recalling the product because the cartridges may contain discs that have an insufficient dose of antibiotic.
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-0808-2013. 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.