Deerfield Imaging, Inc. recalls
Every recall we track for Deerfield Imaging, Inc. — 19 in all, from 2018–2022 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Deerfield Imaging, Inc. peaked in 2018 (13); 19 since 2017.
All FDA recall records for Deerfield Imaging, Inc. since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 13 | 0 | 0 | 13 |
| 2019 | 0 | 2 | 0 | 0 | 2 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 3 | 0 | 0 | 3 |
| 2022 | 0 | 1 | 0 | 0 | 1 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 0 | 0 |
| 2026 (to date) | 0 | 0 | 0 | 0 | 0 |
Most common reasons for Deerfield Imaging, Inc. recalls
What to do if you have a recalled Deerfield Imaging, Inc. product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Deerfield Imaging, Inc. recalls
9 shown- Use cautionMedical device
Deerfield Imaging, Inc. recalls Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation
Deerfield Imaging recalls a table adapter component for IMRIS HFD100 head fixation devices. The split block clamp may deflect after force application, risking unnoticed movement during surgery and extended anesthesia time.
Deerfield ImagingFeb 17, 2022 - Use cautionMedical device
Deerfield Imaging, Inc. recalls Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or
Deerfield Imaging recalls ORT200/300 operating room tables with a rotational lock that may fail to lock or unlock properly, posing a risk of patient injury during procedures.
Deerfield ImagingAug 25, 2021 - Use cautionMedical device
Deerfield Imaging, Inc. recalls iMRX MRI and Angiography System, part number 10094137 and 10094141, a surgical/interventional suite with integrated MRI
Deerfield Imaging recalls iMRX MRI and Angiography Systems with specific part numbers due to potential X-ray tube failure from generator A100 power supply issues. Affected units may not produce X-rays during procedures.
Deerfield ImagingNov 26, 2019 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS MR/X-ray head fixation device, Model HFD200
Deerfield Imaging recalls HFD200 MR/X-ray head fixation devices due to potential improper skull pinning from drive knob force indicator failure. Affected units have specific serial numbers.
Deerfield ImagingJun 26, 2019 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS T2X table, Part Numbers: (a)108000-000, (b)108000-600, (c)109682-000, (d) 109682-600, (e) 110470-600 - Product
Deerfield Imaging recalls IMRIS T2X tables with specific part numbers due to potential drifting in roll position during use. Affected models may require correction to prevent patient positioning issues.
Deerfield ImagingNov 6, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS IMRI 1.5T AND 3T S System Product Usage: The IMRIS intraoperative MRI systems are traditional MRI systems that
Deerfield Imaging recalls IMRIS 1.5T and 3T intraoperative MRI systems due to magnetic field causing IFOSS control panel malfunction. Affected units have specific serial numbers.
Deerfield ImagingApr 4, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS ORT200 Removable Operating Room Table, 50-60 Hz Version is intended for use during diagnostic examinations or
Deerfield Imaging recalls ORT200 operating room tables with serial numbers listed. The rotational locking mechanism may fail to lock, causing unintended movement during procedures.
Deerfield ImagingFeb 23, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS ORT300, Removable Operating Room Table, Part Numbers: (a) 114093-000 (b) 114093-600
Deerfield Imaging recalls IMRIS ORT300 operating room tables with specific part numbers and serials due to potential unintended movement during use. Affected users should contact the manufacturer for details.
Deerfield ImagingFeb 23, 2018 - Use cautionMedical device
Deerfield Imaging, Inc. recalls IMRIS T2X Table, Part Number 109682-600
Deerfield Imaging recalls IMRIS T2X surgical tables with serial numbers listed. The rotational locking may disengage during use, causing unintended table movement. Affected users should contact for remedy.
Deerfield ImagingFeb 20, 2018
Deerfield Imaging, Inc. recall questions
How many recalls has Deerfield Imaging, Inc. had?
19 recalls from Deerfield Imaging, Inc. are on record with U.S. safety agencies, from 2018–2022.
What is the most recent Deerfield Imaging, Inc. recall?
Deerfield Imaging, Inc. recalls Trumpf Mount Clamp Assembly (table adapter component), part #118704-000, a component of the IMRIS HFD100 head fixation, dated Feb 17, 2022. Every Deerfield Imaging, Inc. recall is listed on this page, newest first.
Why are Deerfield Imaging, Inc. products recalled?
The most common reasons on record: Table may drift in the roll position while in use (4).
What should I do if I have a recalled Deerfield Imaging, Inc. product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Deerfield Imaging, Inc. recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.