Devices

Device Recall REMStar Mseries Heated Humidifier System

Model / Serial
Catalog Numbers: 1049109, 1049110, 1049111, and AC1049109.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution -- US including states of OR, OH, KY, TX, MO, AZ, IN and NV and countries of United Arab Emirates, Bosnia, Belgium, Bulgaria, Bahrain, Canada, Czech Republic, Denmark, Egypt, Spain, Finland, Greece, Croatia, Hungary, Ireland, Israel, Jordan, Kuwait, Lebanon, Latvia, Macedonia, Netherlands, Norway, Oman, Poland, Portugal, Romania, Qatar, Russia, Slovenia, Turkey, Serbia and South Africa.
Product Description
Remstar Pro M-Series Heated Humidifier System.
Manufacturer
Respironics
1 Event
- Recall of Device Recall REMStar Mseries Heated Humidifier System

Manufacturer

Respironics

Manufacturer Address
Respironics, 1740 Golden Mile Hwy, Monroeville PA 151462012
Manufacturer Parent Company (2017)
Philips
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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