Nipro Safe Touch TULIP Safety Fistula Needle recall
Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring…
Why was Nipro Safe Touch TULIP Safety Fistula Needle recalled?
Some 1 1/4" needles were packaged and labeled in the 1" blister package.
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?
Lot # 15C03
- Product
- Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring…
- Recalling firm
- Nipro Medical Corporation
- Quantity
- 50,000 pieces
- Distribution
- Indiana
- Recall date
- November 4, 2015
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)