PlainRecalls
FDA Devices Moderate Class II Terminated

DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS

Reported: June 24, 2020 Initiated: April 30, 2020 #Z-2402-2020

Product Description

DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS

Reason for Recall

Incorrect labeling of dialysate concentration for hemodialysis.

Details

Recalling Firm
Diasol, Inc
Units Affected
212 Cases of 4 gallons each
Distribution
U.S.: CA O.U.S.:None
Location
Phoenix, AZ

Frequently Asked Questions

What product was recalled?
DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS. Recalled by Diasol, Inc. Units affected: 212 Cases of 4 gallons each.
Why was this product recalled?
Incorrect labeling of dialysate concentration for hemodialysis.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 24, 2020. Severity: Moderate. Recall number: Z-2402-2020.