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Nakao Quicktrap

STRYKER CORPORATION · Model 0700050000 · UDI-DI 04546540510952

BYZ Prescription
9
510(k) clearances
26
Adverse events
1
Recalls
63
Facilities

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

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.