Drug recall

Diasol Acid Concentrate REF G100325-10Dex 100

FDA recall event 95334 · Class II · Diasol, Inc

Key facts

Event ID 95334
Recall numbers Z-0207-2025
Recalling firm Diasol, Inc
Product type Devices
Products Diasol Acid Concentrate REF G100325-10Dex 100
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Due to labeling issue. The box label is different that the gallon label in that gallon label shows a lower Calcium concentration than the box label.
Initiation date Jul 27, 2022
Report date Oct 30, 2024
City Phoenix
State AZ
Country United States
FEI number 3007137482

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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