Devices

Device Recall Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor

Model / Serial
Product Code: 003-40C, Lot numbers: 109127, 155127, 157127, 174127, 195127, 222127, 277127, 335127, 337127, 384127, 422127, 425127, 497127 & 500127.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Belgium, Canada, China, Germany, Great Britain, France, India, Malaysia, Mexico, Philippines, Singapore, Thailand and Zambia.
Product Description
Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
Manufacturer
Teleflex Medical
1 Event
- Recall of Device Recall Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor

Manufacturer

Teleflex Medical

Manufacturer Address
Teleflex Medical, 4024 Stirrup Creek Dr, Durham NC 27703-9000
Manufacturer Parent Company (2017)
Teleflex Incorporated
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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