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Myo Munchee

MYO MUNCHEE (OPERATIONS) PTY LTD · Model 1 · UDI-DI 09359648000004

ION
10
510(k) clearances
116
Adverse events (2 deaths)
2
Recalls
255
Facilities

Description

MYO MUNCHEE BEBE - reusable oral insert - BEBE 2 Piece

Recalls

DateFirmReason
2015-03-27Amtryke LLCProduct is being recalled due to complaints of cracked frames.
2011-07-11North Coast Medical IncPotential for plastic D-ring to break during use and cause injury.

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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.