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Device Recall ILLINOIS (TJ) NEEDLE ASPIRATION
Model / Serial
Product Code: a.) TIN3015/ LOT 0000836578, 0000841213, 0000841215, 0000842719, 0000842721, 0000845423, 0000848061, 0000849715, 0000850938, 0000852076, 0000854859; Product Code: b.) TIN3018/ LOT 0000836574, 0000841212, 0000852078
Product Classification
General and Plastic Surgery Devices
Device Class
1
Implanted device?
No
Distribution
Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam
Product Description
ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;
Manufacturer
Carefusion 2200 Inc
1 Event
Recall of Device Recall ILLINOIS (TJ) NEEDLE ASPIRATION
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Manufacturer
Carefusion 2200 Inc
Manufacturer Address
Carefusion 2200 Inc, 75 N Fairway Dr, Vernon Hills IL 60061-1845
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA
Language
English
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