Diasol, Inc: Medical Device Recall in 2020 - (Recall #: Z-2402-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: April 30, 2020

Date Posted: June 24, 2020

Recall Number: Z-2402-2020

Event ID: 85695

Reason for Recall:

Incorrect labeling of dialysate concentration for hemodialysis.

Status: Terminated

Product Quantity: 212 Cases of 4 gallons each

Code Information:

Model Number: 100225-10-DEX100 Gallons Unique Device Identifier (UDI): B467100225101004 and B4671000225101004 Lot codes if applicable: PHQ03041/030920

Distribution Pattern:

U.S.: CA O.U.S.:None

Voluntary or Mandated:

Voluntary: Firm initiated