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Percussionaire - safety alert

Official notice

29 Jan 2025

CriticalFDA

An official FDA notice concerns Percussionaire. The notice reports a health risk requiring medical assessment. Stop using the product and follow the official notice. Published 2025-01-29. Models: -, A51001, PRT. Recall numbers: Z-0960-2025. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

4,727

Recall number

Z-0960-2025

Official notice

2025-01-29

The hazard

Health risk requiring medical assessment

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

-, A51001, PRT

Other

UDI-DI 00849436000259

Event Ids

95979

Model Numbers

-, A51001, PRT

Recall Numbers

Z-0960-2025

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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

Affected area 1

US · United States

Affected area 2

BE · Belgium

Affected area 3

CA · Canada

Affected area 4

CH · Switzerland

Affected area 5

FR · France

Affected area 6

HK · Hong Kong

Affected area 7

NL · Netherlands

Affected area 8

RU · Russia

Affected area 9

TR · Turkey

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Percussionaire. Contact: Percussionaire Corporation.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class I

App estimate

critical

Recall details

Recall number

Z-0960-2025

Event id

95979

Units affected

4,727

Status

active

Classification

Class I

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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