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Monaghan Medical Corporation

Monaghan Medical Corporation · Model Filtered Mouthpiece, cs/50 · UDI-DI 00604351600515

BYW
2
510(k) clearances
29
Adverse events
1
Recalls
30
Facilities

Recalls

DateFirmReason
2006-10-31Teleflex MedicalMislabeling-The rebreathing bag is incorrectly labeled as a 1 liter bag when it is actually a 1/2 liter bag.

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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.