Fresh Recalls

FDAClass II · Medical device · Recall Z-3033-2026 · Recalled September 2, 2026

ORT200 recall — IMRIS Imaging Inc

Agency report date: September 2, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
ORT200
Company / brand
IMRIS Imaging
Lot / serial / date codes
113821-600 - Serial Numbers: 10003754, 10006997; 114148-000 - UDI-DI: 00857534006349, Serial Numbers: 10005189, 10005190, 10004463, 10004997
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.
Agency product description and boundaries

ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: ORT200 recall status

3. Open the official notice or contact

Official recall ID
Z-3033-2026
Brand
All IMRIS Imaging recalls
Classification
Class II
Units affected
6 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Chaska, MN, United States
Firm address
1230 Chaska Creek Way Ste 100, N/A, 55318-2707

Identifying details (verbatim from the notice)

Product codes / lots
113821-600 - Serial Numbers: 10003754, 10006997; 114148-000 - UDI-DI: 00857534006349, Serial Numbers: 10005189, 10005190, 10004463, 10004997
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, China, Japan, Sweden.
Firm notified the public via
N/A
FDA event ID
99596
Recall initiated
August 6, 2026
FDA classified
August 26, 2026
FDA report date
September 2, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved October 22, 2026 at 6:00 PM UTC.

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