No image published for this recall

ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50 60Hz

Official notice

2 Sept 2026

Last checked

22 Sept 2026

MediumFDA

An official FDA notice concerns Imris Imaging. The notice reports an injury risk. Stop using the product and follow the official notice. Published 2026-09-02. Recall numbers: Z-3033-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

6

Recall number

Z-3033-2026

Official notice

2026-09-02

The hazard

Injury risk

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 00857534006349

Event Ids

99596

Recall Numbers

Z-3033-2026

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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

CA · Canada

Affected area 3

CN · China

Affected area 4

JP · Japan

Affected area 5

SE · Sweden

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Imris Imaging. Contact: IMRIS Imaging Inc.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-3033-2026

Event id

99596

Units affected

6

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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