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BD Kiestra LAB Automation recalls

BD Kiestra LAB Automation has 1 recall on record with the FDA and USDA, the earliest in 2026 and the latest reported on 8 Apr 2026. 1 is still ongoing. 1 was reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls1since 2026

Last 12 months1reported

Class I00% of total

Ongoing1latest 8 Apr 2026

Recalls per month, last 24 months

click a bar for that month

0Nov '24 0 0 0Feb 0 0 0May 0 0 0Aug 0 0 0Nov 0 0 0Feb 0 1 0May 0 0 0Aug 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why bd kiestra lab automation is recalled

Potency & Assay1100%

Product types

Other Medical Devices1100%

By year

20261100%

Ongoing bd kiestra lab automation recalls

1 active

Reported	Class	Recall	Company	Reason	Where
8 Apr 2026Device	CLASS II	BD Kiestra" ReadA recalled	BD Kiestra LAB Automation	Potency & Assay	6 states

All bd kiestra lab automation recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
8 Apr 2026Device	CLASS II	BD Kiestra" ReadA recalled	BD Kiestra LAB Automation	Potency & Assay	6 states

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.