Tubing Change KIT recall
TUBING CHANGE KIT
Why was Tubing Change KIT recalled?
Convenience Kit contains a PVP Prep Pad, received by a supplier, that does not meet the iodine assay level required to support the 36 month shelf life.
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?
DT6870 Lot codes: 2015110290 2016090890 2017042690
- Product
- TUBING CHANGE KIT
- Recalling firm
- Centurion Medical Products Corporation
- Quantity
- N/A
- Distribution
- Nationally
- Recall date
- March 28, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)