The Recall Desk

Manufacturer

Deerfield Imaging

2 recalls in our database name Deerfield Imaging as the manufacturing or recalling firm.

What the numbers show

Total
2
Critical
0
Severe
0
Most recent
2017-10-04

Of the 2 recalls from Deerfield Imaging we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 0 (0%) are Severe.

About this listing

The manufacturer string comes from the agency’s own source notice — for FDA recalls, the “recalling firm” field; for NHTSA recalls, the vehicle manufacturer; for CPSC recalls, the firm-of-record on the joint press release. A single corporate family can appear under multiple manufacturer strings as agency notices aren’t standardized on a canonical name. If you don’t see recalls you expect, try a parent-company search or a broader full-text search.

Severity scores below are computed from the agency’s classification and the recall text, never from manufacturer behaviour or history. Many manufacturers issue routine corrective actions (software updates, labelling corrections) that are correctly scored low — having recalls on this list isn’t inherently a quality signal.

1–2 of 2

  • ModerateFDA (Devices)·Z-3211-2017·2017-10-04

    Deerfield Imaging Recalls Starburst Adaptor Thumb Screws Due to Incorrect Thread

    Deerfield Imaging is recalling six Starburst adaptor thumb screws because they have incorrect threads. The affected units were distributed in Illinois, Oregon, and Pennsylvania.

    Product
    IMRIS DEERFIELD IMAGING, REF 113803, Starburst adaptor thumb screw
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1098-2016·2016-03-23

    Deerfield Imaging Recalls Intraoperative MRI Systems Due to Venting Line Defect

    Deerfield Imaging is recalling specific intraoperative MRI systems because emergency helium venting lines may not have been properly installed.

    Product
    Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic resonance diagnostic device (MRDD).
    Category
    Medical Device
    Distribution
    19 states