Becton, Dickinson and Company, BD Bio Sciences

Complete recall history across all FDA and CPSC categories — 10 total recalls

Becton, Dickinson and Company, BD Bio Sciences appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (10)

FDA medical device enforcement actions by Becton, Dickinson and Company, BD Bio Sciences

Date Product Reason Class
Jul 8, 2025 BD Trucount Controls, 30 Test - REF: 340335 Control kits contain incorrect standard deviation (SD) values for the low and... Class II
Jul 8, 2025 BD Trucount Controls, 30 Test - REF: 664343, RxOnly, IVD Control kits contain incorrect standard deviation (SD) values for the low and... Class II
Jun 3, 2025 REF: 335775 , BD FACS, 7-Color Setup Beads, 25 setups per kit, Rx Only, IVD. ... Due to customer complaints, errors in spectral overlap factors table for 7-c... Class II
Jun 3, 2025 REF: 666289 , BD FACS, 7-Color Setup Beads, 25 Runs, CE, IVD. Used in flow cy... Due to customer complaints, errors in spectral overlap factors table for 7-c... Class II
Nov 1, 2024 Device Description: FACSLyric 2L6C Instrument US, Catalog Number 662876, U... On October 18, 2024, BD has identified through customer complaints and an inc... Class II
Nov 1, 2024 FACSLyric 3L8C Instrument US-IVD, Catalog Number 662877, UDI 00382906628770 ... On October 18, 2024, BD has identified through customer complaints and an inc... Class II
Nov 1, 2024 FACSLyric 3L10C Instrument US-IVD, Catalog Number 662878, UDI 00382906628787 ... On October 18, 2024, BD has identified through customer complaints and an inc... Class II
Nov 1, 2024 FACSLyric 3L12C Instrument RUO, Catalog Number 663518, UDI 00382906635181 On October 18, 2024, BD has identified through customer complaints and an inc... Class II
Nov 1, 2024 FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD... On October 18, 2024, BD has identified through customer complaints and an inc... Class II
Aug 12, 2024 BD FACSDuet Premium Sample Preparation System, REF: 666340, 666339; and BD FA... Sample preparation system with software may cause: 1) Multidispense feature e... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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