Deerfield Imaging, Inc.

FDA recalling firm · 9 enforcement events · 19 product records · 2018–2022 · MN

Deerfield Imaging, Inc. has 9 FDA enforcement events on this register (19 product records) between 2018 and 2022: 9 device; the busiest year was 2018 with 5.

0% of its events are Class I; the most common class is Class II (9). 0 events are listed as ongoing; the recalling firm's address is in MN.

Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.

Enforcement events

Initiated	Product (first record)	Type	Class	Records	Status
17 Feb 2022	Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation device, models #119629-000 and #119630-000, which are used with ORT400 operating room tables.	Device	Class II	1	Terminated
25 Aug 2021	Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.	Device	Class II	3	Terminated
26 Nov 2019	iMRX MRI and Angiography System, part number 10094137 and 10094141, a surgical/interventional suite with integrated MRI and X-ray angiography. The IMRIS iMRX system is the integration of a Siemens Artis zee family (biplane or floor or ceiling mounted single plane) and the IMRIS Neuro 3T System. The System is a…	Device	Class II	1	Terminated
26 Jun 2019	IMRIS MR/X-ray head fixation device, Model HFD200	Device	Class II	1	Terminated
6 Nov 2018	IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product Usage: The ORT200 and ORT300 are intended for use during diagnostic examinations, radiologic procedures, or surgical procedures to support and position a patient. The tables are indicated for imagining…	Device	Class II	4	Terminated
4 Apr 2018	IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditional MRI systems that have been suspended on an overhead rail system. and is designated to operative inside an RF shielded room to facilitate intraoperative and multi room use.	Device	Class II	1	Terminated
23 Feb 2018	IMRIS ORT200 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or surgical procedures to support and position a patient.	Device	Class II	2	Terminated
23 Feb 2018	IMRIS ORT100 Table, Part Numbers: (a) 110470-000 (b) 110470-600	Device	Class II	4	Terminated
20 Feb 2018	IMRIS ORT100 Table, Part Number 110470-000	Device	Class II	2	Terminated

By type and class

Device9

Class II9

Class I: 0% of this firm's events; 18% of all events on the register.

Events by year

Enforcement events for Deerfield Imaging, Inc. by year initiated.

Questions and answers

How many FDA recalls has Deerfield Imaging, Inc. had?

9 enforcement events (19 product records) on this register, 2018–2022: 9 device.

Are any Deerfield Imaging, Inc. recalls ongoing?

0 events are listed as ongoing in the current openFDA export.

What class are Deerfield Imaging, Inc. recalls?

9 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.

Where does this data come from?

openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.

Provenance

Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.