International safety notice

Bausch Lomb ReNu läätsehooldusvedelik - tagasikutsumine, steriilsus ei ole tagatud

Estonia / EMDDB · EST · May 1, 2021

Key facts

Title Bausch Lomb ReNu läätsehooldusvedelik - tagasikutsumine, steriilsus ei ole tagatud
Regulator Estonia / EMDDB
Country EST
Brand Bausch Lomb ReNu läätsehooldusvedelik
Manufacturer BAUSCH LOMB RENU LÄÄTSEHOOLDUSVEDELIK
Models MF2679, MF1495, MF1438, 44-20-8089-3775, ME4359, 44-20-8705-0539, ME2440, ME4247, MF1869, MF2368, ME4643, ME4512 and 2 more
Date May 1, 2021
Regulator page terviseamet.ee

At a glance

  • No Recall
  • No Field safety notice

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices