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Percussionaire - safety alert

Official notice

22 Oct 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 2025-10-22. Recall numbers: Z-0031-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

59,160

Recall number

Z-0031-2026

Official notice

2025-10-22

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.

Other

UDI-DI 00849436000723

Event Ids

97374

Recall Numbers

Z-0031-2026

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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

AE · United Arab Emirates

Affected area 3

CA · Canada

Affected area 4

CH · Switzerland

Affected area 5

CL · Chile

Affected area 6

GB · United Kingdom

Affected area 7

IL · Israel

Affected area 8

JP · Japan

Affected area 9

RU · Russia

Affected area 10

TR · Turkey

Affected area 11

ZA · South Africa

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-0031-2026

Event id

97374

Units affected

59,160

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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