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Pump, Infusion, Analytical Sampling

FDA product code LZF · Class 2 · General Hospital

2
Registered devices
2
Adverse events
1
Recalls
7
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-05-24International Biomedical, Ltd.International Biomedical has received reports of interference between the collection bag and the extension set connectors. Evaluation of the affected components

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.