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SUCTION TUBE

KLS-Martin L.P. · Model 00-102-59-07 · UDI-DI 00888118002525

KCB Prescription
1
510(k) clearances
8
Adverse events
1
Recalls
109
Facilities

Description

TONSIL, WALLACE

Recalls

DateFirmReason
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma

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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.