FDA Medical devices recall ·
Diasol Acid Concentrate recall
- Recall number
- Z-0207-2025
- Date
- (initiated July 27, 2022)
- Company / brand
- Diasol, Inc
310 S 43rd Ave Ste B, Phoenix, AZ, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 852 gallon bottles
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Diasol Acid Concentrate REF G100325-10Dex 100
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
Catalog Number: G100325-10Dex100 UDI code: B467100325101004 Lot Number:PHS06011/061722
Distribution
U.S. Nationwide distribution in the state of AZ.
States: Arizona
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0207-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.