Hudson Respiratory Care, Inc.
United StatesFDA applicant, unverified
- Devices
- 15
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
Catalogue
Search and filter all 15 devicesFDA recalls
2004
- 20 Apr 2004 Z-0929-04 Unclassified (pre-2012) Terminated Software malfunction. The humidifier did not retain the clinician selected default settings for temperature gradient, after the unit had been placed in the "pause" mode.
Frequently asked questions
How many devices does Hudson Respiratory Care, Inc. have in the registry?
The registry currently lists 15 devices for Hudson Respiratory Care, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hudson Respiratory Care, Inc.'s devices?
Among its 15 most recently registered devices, Hudson Respiratory Care, Inc. has devices listed in FDA 510(k) (15 devices).
What risk classes do Hudson Respiratory Care, Inc.'s devices fall under?
Among its 15 most recently registered devices, the classes recorded for Hudson Respiratory Care, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Hudson Respiratory Care, Inc.?
FDA recall records list 1 recall initiated by Hudson Respiratory Care, Inc., the most recent initiated on 20 Apr 2004. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Hudson Respiratory Care, Inc. in the registry?
The most recently registered devices listed for Hudson Respiratory Care, Inc. include DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA, CONCHATHERM IV HEATED MOLECULAR HUMIDIFIER, SMOOTH-FLO CIRCUIT and MODEL 780.