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Horiba Instruments Dba Horiba Medical - safety alert

Official notice

4 Jul 2018

Last checked

4 Jul 2018

Medium riskFDA

An official FDA notice concerns Horiba Instruments Dba Horiba Medical - safety alert. An official FDA notice concerns Horiba Instruments Dba Horiba Medical. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-07-04. Recall numbers: Z-2286-2018. Check the official notice for the complete list. Published 2018-07-04.

What to do now

The source does not provide specific consumer instructions. Follow the official FDA notice for next steps.

Units affected

686

Recall number

Z-2286-2018

Official notice

2018-07-04

The hazard

An official FDA notice concerns Horiba Instruments Dba Horiba Medical. The notice reports a product safety risk. Follow the official notice for consumer instructions. Published 2018-07-04. Recall numbers: Z-2286-2018. Check the official notice for the complete list.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Event Ids

80022

Recall Numbers

Z-2286-2018

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States · CA · Irvine

Affected area 1

US · United States · CA · Irvine

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Horiba Instruments Dba Horiba Medical. Contact: Horiba Instruments, Inc dba Horiba Medical.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-2286-2018

Event id

80022

Units affected

686

Status

terminated

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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