Devices

Device Recall Baker Jejunostomy Tubes:

Model / Serial
(a) 655300160 655316 Batch Numbers 13EG28 13HG23 (b) 655500200 655520 Batch Numbers: 13EG28
Product Classification
Gastroenterology-Urology Devices
Device Class
2
Implanted device?
No
Distribution
US Nationwide Distribution
Product Description
Baker Jejunostomy Tubes: || Product Code Equivalent Code || (a) 655300160 655316 || (b) 655500200 655520
Manufacturer
Teleflex Medical Europe Ltd
1 Event
- Recall of Device Recall Baker Jejunostomy Tubes:

Manufacturer

Teleflex Medical Europe Ltd

Manufacturer Address
Teleflex Medical Europe Ltd, Ida Business Park, Athlone Ireland
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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