Z-0932-2022 Class II Terminated
FDA device recall Z-0932-2022 was initiated by MEDLINE INDUSTRIES, LP - Northfield on Mar 8, 2022 and is designated Class II. Reason for recall: Product was improperly store which may cause a delay in results. The recall status is terminated (terminated Mar 20, 2023). Affected quantity: 45 ea.
Recall Details
- Product Type
- Devices
- Report Date
- Apr 20, 2022
- Initiation Date
- Mar 8, 2022
- Termination Date
- Mar 20, 2023
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 45 ea
Product Description
Hydroxybutyrate LiquiColor Tests - includes 3 bottles (1 of each size, 3mL, 8.5mL, and 50mL)
Reason for Recall
Product was improperly store which may cause a delay in results.
Distribution Pattern
US distribution only - AL, CA, FL, GA, IL, IN, LA, MO, MS, NC, NE, NY, OH, PA, VA, and WA
Code Information
Model/Item No. S-O2440058; Lots 171793, 169614, 167181, 171713 UDI: 00657498000519
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0932-2022
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 26, 2026