International safety notice

Recall for Birdie Patient Hoist, Invacare Aquatec

Germany / BfArM · DEU · Jul 24, 2009

Key facts

Title Recall for Birdie Patient Hoist, Invacare Aquatec
Regulator Germany / BfArM
Country DEU
Brand Birdie Patient Hoist, Invacare Aquatec
Manufacturer Recall for Birdie Patient Hoist, Invacare Aquatec
Models 00-36, 88316, 010903762281001, 010802716382001
Date Jul 24, 2009
Regulator page bfarm.de

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