⚠ RecallRadar📷 ScanGuidesOfficial U.S. recall notices, restated plainly

Becton Dickinson & Co.: BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;

Medical DevicesSource: FDA (device) · Date: 2025-11-19

Read the official notice at FDA (device) →

Share on XFacebookRedditEmail

Get alerts for Becton Dickinson &

Guides: Which agency handles which recall (FDA vs USDA vs CPSC vs NHTSA)

The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.

Company / brand
Becton Dickinson & Co.
Product
BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
Reason / hazard
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
Status
Ongoing
Distribution / sold at
Worldwide - US Nationwide distribution in the states of CO, CT, KY, NJ, TN, TX, UT and the countries of Belgium, Singapore, Taiwan, Germany, Switzerland.
Recall initiated
2025-10-23
Code info
Catalog No.: 246100; UDI-DI: 30382902461006; Lot Number: LM245590, LM245592, LM245593, LM245594, LM245666;
Product quantity
29,760 units
Voluntary mandated
Voluntary: Firm initiated
City
Sparks
State
MD
Country
United States
Event id
97817
Free daily digest + "My products" watchlist

Get the daily digest, and tell us what to watch. Everything is optional except your email.

Free allergen alerts:

Categories:

Privacy: we store only what you enter here, use it only to send recall alerts you asked for, never sell or share it, and you can unsubscribe anytime. Double opt-in: we will email you a confirmation link before sending anything; alerts start only after you confirm. Every email has unsubscribe and manage-watchlist links.