Becton Dickinson & Co. recalls BD Kiestra" Isolate Suspension Cuvette Array
- Recalling company
- Becton Dickinson & Co.
- Product
- BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
- Reason
- The 2D barcodes on these cuvettes contain formatting errors that prevent the analyzing system from correctly reading the expiration date. As a result, the instrument enters an error state and the cuvettes cannot be used.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Oct 23, 2025
- Reported
- Nov 19, 2025
- Distribution
- Worldwide - US Nationwide distribution in the states of CO, CT, KY, NJ, TN, TX, UT and the countries of Belgium, Singapore, Taiwan, Germany, Switzerland.
- Status
- Ongoing
- Quantity
- 29,760 units
- Lot / codes
- Catalog No.: 246100; UDI-DI: 30382902461006; Lot Number: LM245590, LM245592, LM245593, LM245594, LM245666;
- Company location
- Sparks, MD
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-0484-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-0484-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.