Illinois recall
ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;
Why was Illinois recalled?
The integrity of the sterile packaging is potentially compromised.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
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
- ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;
- Recalling firm
- Carefusion 2200 Inc
- Quantity
- a.) 13,010 units b.) 2116 units
- Distribution
- Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam
- Recall date
- April 25, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)