Mercury Enterprises, Inc. dba Mercury Medical

FDA Regulatory Profile

Mercury Enterprises, Inc. dba Mercury Medical appears in FDA public data with 3 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-0821-2025, Class I) was initiated on December 10, 2024.

Summary

Total Recalls
3 (2 Class I)
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-0821-2025Class INeo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1December 10, 2024
Z-0004-2025Class INeo-Tee T-Piece Resuscitator. Part Numbers 1050805, 1050832. For pediatric emergency respiratory supAugust 30, 2024
Z-0639-2016Class IIMercury Medical Neo-Tee T-Piece Resuscitator and T-Piece Circuit. The Neo-Tee T-Piece Resuscitator October 22, 2015