Horiba Instruments Incorporated recalls

Horiba Instruments Incorporated has 2 recalls on record with the FDA and USDA, the earliest in 2019 and the latest reported on 10 Jul 2024. 1 is still ongoing. The most frequent reason is foreign material.

Total recalls2since 2019

Last 12 months0reported

Class I00% of total

Ongoing1latest 10 Jul 2024

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 0 0

Severity split

Class I 0 0%Class II 2 100%Class III 0 0%

Why horiba instruments incorporated is recalled

Foreign Material150%
Other Reasons150%

Product types

Other Medical Devices2100%

By year

2024150%
2019150%

Ongoing horiba instruments incorporated recalls

1 active

Reported	Class	Recall	Company	Reason	Where
10 Jul 2024Device	CLASS II	Horiba custom configured fluorescence instrument recalled	Horiba Instruments Incorporated	Foreign Material	Nationwide

All horiba instruments incorporated recalls, newest first

2 total

Reported	Class	Recall	Company	Reason	Where
10 Jul 2024Device	CLASS II	Horiba custom configured fluorescence instrument recalled	Horiba Instruments Incorporated	Foreign Material	Nationwide
16 Oct 2019Device	CLASS II	Clinical Chemistry, ABX Pentra Lipase CP, ABX Pentra 400/Pentrac400 recalled	Horiba Instruments Incorporated	Other	40 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.