Home › Device types › KZI
Culture Media, Enriched
FDA product code KZI · Class 1 · Microbiology
153
Registered devices
3,141
Adverse events
2
Recalls
51
510(k) clearances
Devices with this code
N/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSAnaeroGRO — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSPRAS Anaerobic Enrichment Broth (MTGE BROTH) — ANAEROBE SYSTEMSBD BBL™ Lowenstein-Jensen Medium Mycoflask™ — BECTON, DICKINSON AND COMPANYBD BBL™ Sabouraud Dextrose Agar, Emmons (Deep Fill) — BECTON, DICKINSON AND COMPANYN/A — HARDY DIAGNOSTICSBD BBL™ Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitaleX™) — BECTON, DICKINSON AND COMPANYN/A — HARDY DIAGNOSTICSBD BBL™ GN Broth — BECTON, DICKINSON AND COMPANYN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSHardyCHROM — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSN/A — HARDY DIAGNOSTICSPRAS BRU PEA LKV Convenience Pack — ANAEROBE SYSTEMSPRAS Brucelle Blood Agar (BRU) — ANAEROBE SYSTEMS
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-02-19 | Becton Dickinson & Co. | In vitro diagnostic test reagent may contain residual material that inhibits the growth of gram positive/gram negative organisms. |
| 2004-09-27 | Remel, Inc. | The product does not perform as intended with some quality control organisms (Haemophilus influenzae) |
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