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Trap, Sterile Specimen

FDA product code BYZ · Class 2 · General Hospital

59
Registered devices
23
Adverse events
1
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2013-11-04Medline Industries IncThere is a potential that the specified mucus specimen traps are not sterile. Use of the affected products may result in the contamination of patient specimens.

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