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No image published for this recall

GE Healthcare Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019 - safety alert

Official notice

6 Jul 2022

Last checked

6 Jul 2022

Medium riskFDA

An official FDA notice concerns GE Healthcare Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019 - safety alert. An official FDA notice concerns Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2022-07-06. Models: 1009-9050-000. Recall numbers: Z-1285-2022. Check the official notice for the complete list. Published 2022-07-06.

What to do now

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

Units affected

6,612

Recall number

Z-1285-2022

Official notice

2022-07-06

The hazard

An official FDA notice concerns Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2022-07-06. Models: 1009-9050-000. Recall numbers: Z-1285-2022. 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.

Skus

1009-9050-000

Event Ids

90137

Model Numbers

1009-9050-000

Recall Numbers

Z-1285-2022

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Affected products

Product 1

Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019

Units affected

6,612

Risk / hazard

An official FDA notice concerns Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2022-07-06. Models: 1009-9050-000. Recall numbers: Z-1285-2022. Check the official notice for the complete list.

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 · WI · Waukesha

Affected area 1

US · United States · WI · Waukesha

Affected area 2

US · United States

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: GE Healthcare. Contact: GE Healthcare, LLC.

Source & status

Source

Tier

official

Category

ELECTRONICS

App estimate

medium

Recall details

Recall number

Z-1285-2022

Event id

90137

Units affected

6,612

Status

active

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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