stay-safe /Luer Catheter Ext. 6 in recall
stay-safe /Luer Catheter Ext. 6 in
Why was stay-safe /Luer Catheter Ext. 6 in recalled?
The peroxide cross-linked tubing has leachables identified as NDL PCBAs.
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA 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?
Model Number: 050-95013; UDI/DI (Bag): 00840861100804; UDI/DI (Case): 10840861100801; All lots.
- Product
- stay-safe /Luer Catheter Ext. 6 in
- Recalling firm
- Fresenius Medical Care Holdings, Inc.
- Quantity
- 105,700 eaches
- Distribution
- Domestic: Nationwide Distribution.
- Recall date
- April 3, 2024
- Classification
- Class I
- Status
- Ongoing
- Agency
- FDA (device)