Devices

Device Recall Arterial Catheterization Set

Model / Serial
Product # CK-04018, Lot No's: RF0019104 and RF0022537
Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
The product was shipped to medical centers and hospitals nationwide and to Australia, New Zealand, and Europe.
Product Description
Arterial Catheterization Set
Manufacturer
Arrow International Inc
1 Event
- Recall of Device Recall Arterial Catheterization Set

Manufacturer

Arrow International Inc

Manufacturer Address
Arrow International Inc, 2400 Bernville Road, Reading PA 19605
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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