Z-1841-2025 Class II Ongoing
FDA device recall Z-1841-2025 was initiated by Mckesson Medical-Surgical Inc. Corporate Office on Apr 24, 2025 and is designated Class II. Reason for recall: transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the… The recall status is ongoing. Affected quantity: 1 unit.
Recall details
- Product Type
- Devices
- Report Date
- Jun 4, 2025
- Initiation Date
- Apr 24, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1 unit
Product description
ABBOTT DIAGNOSTICS PROBE CONDITIONING F/ARCHITECT ANLYZ ABBDIA SOLUTION.
Reason for recall
transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.
Distribution pattern
US Nationwide distribution in the states of AL, AR, IL, KS, MT, NC, NJ, OR, SC, TN & WV.
Code information
Catalog No. 01L5640; GTIN: 380740001193; Order No. 46048552.
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1841-2025
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026