Reported Jun 24, 2020 · Terminated

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

Diasol, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Diasol, Inc · 310 S 43rd Ave Ste B · Phoenix, AZ · 85009-4606

Is this the product you have?

  • DIASOL 1000225-10-DEX100 LIQUID ACID CONCENTRATE FOR BICARBONATE DIALYSIS
Lot codes and dates
  • Model Number100225-10-DEX100
  • Gallons Unique Device Identifier (UDI)B467100225101004 and B4671000225101004
  • Lot codes if applicablePHQ03041/030920
Amount recalled
212 Cases of 4 gallons each

Where it was sold

Why it was recalled

Incorrect labeling of dialysate concentration for hemodialysis.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated May 28, 2024 · Data as of Sep 19, 6:13 PM UTC

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