VersaSafe Extension Set recall
VersaSafe Extension Set, Model No. 21000M-007
Why was VersaSafe Extension Set recalled?
CareFusion is recalling the VersaSafe Extension Intravascular Administration Set because it may have excessive adhesive which will prevent the male spin collar to operate as intended.
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 No. 13066550
- Product
- VersaSafe Extension Set, Model No. 21000M-007
- Recalling firm
- CareFusion 303, Inc.
- Quantity
- 3500 units
- Distribution
- Nationwide Distribution.
- Recall date
- December 11, 2013
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)