Beckman Coulter Biomedical recalls

Beckman Coulter Biomedical has 7 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 12 Aug 2026. 6 are still ongoing. 1 was reported in the last 12 months. The most frequent reason is foreign material.

Total recalls7since 2020

Last 12 months1reported

Class I00% of total

Ongoing6latest 12 Aug 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 1 0

Severity split

Class I 0 0%Class II 7 100%Class III 0 0%

Why beckman coulter biomedical is recalled

Product types

By year

2026114%
2024343%
2023229%
2020114%

Ongoing beckman coulter biomedical recalls

6 active

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Remisol Advance recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Potency & Assay	5 states
11 Sep 2024Device	CLASS II	PE Centrifuge recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Foreign Material	Nationwide
11 Sep 2024Device	CLASS II	Power Express recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Foreign Material	Nationwide
11 Sep 2024Device	CLASS II	PE Centrifuge Temperature Controlled recalled	Beckman Coulter Biomedical	Foreign Material	Nationwide
26 Jul 2023Device	CLASS II	Beckman Coulter DxA Automation System, DxA recalled	Beckman Coulter Biomedical	Device Malfunction	17 states
26 Jul 2023Device	CLASS II	Beckman Coulter DxA Automation System, DxA 5000 Fit recalled	Beckman Coulter Biomedical	Device Malfunction	17 states

All beckman coulter biomedical recalls, newest first

7 total

Reported	Class	Recall	Company	Reason	Where
12 Aug 2026Device	CLASS II	Remisol Advance recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Potency & Assay	5 states
11 Sep 2024Device	CLASS II	PE Centrifuge recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Foreign Material	Nationwide
11 Sep 2024Device	CLASS II	Power Express recalled by Beckman Coulter Biomedical	Beckman Coulter Biomedical	Foreign Material	Nationwide
11 Sep 2024Device	CLASS II	PE Centrifuge Temperature Controlled recalled	Beckman Coulter Biomedical	Foreign Material	Nationwide
26 Jul 2023Device	CLASS II	Beckman Coulter DxA Automation System, DxA recalled	Beckman Coulter Biomedical	Device Malfunction	17 states
26 Jul 2023Device	CLASS II	Beckman Coulter DxA Automation System, DxA 5000 Fit recalled	Beckman Coulter Biomedical	Device Malfunction	17 states
30 Sep 2020Device	CLASS II	DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage recalled	Beckman Coulter Biomedical	Potency & Assay	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.