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MTEHFYAF

Beijing Xingjian Yongzhen Technology Co. , Ltd. · Model MY-QYJ-01 · UDI-DI 06975029700078

BYW
2
510(k) clearances
29
Adverse events
1
Recalls
31
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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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.