DriSate¿ recall
DriSate¿ Product Code DR-145 The acid concentrate powders and liquids are indicated for use in acute and chronic hemodialysis and to be used with the…
Why was DriSate¿ recalled?
A subassembly component (dextrose bag) within this case product contained small amounts of sodium bicarbonate from a prior batch.
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 28562-0220171
- Product
- DriSate¿ Product Code DR-145 The acid concentrate powders and liquids are indicated for use in acute and chronic hemodialysis and to be used with the…
- Recalling firm
- Rockwell Medical, Inc
- Quantity
- 139
- Distribution
- US Distribution to the state of NY
- Recall date
- May 23, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)