Reported Aug 29, 2012 · Terminated

GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. In certain fluoroscope X-ray modes, the cable provides…

GE OEC Medical Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: GE OEC Medical Systems, Inc · 384 Wright Brothers Dr · Salt Lake City, UT · 84116-2862

Is this the product you have?

  • GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. In certain fluoroscope X-ray modes, the cable provides a signal to the auto-injector to trigger a contrast injection. Part numbers include 00-902260-01 and 00-883654-01.
Lot codes and dates
  • Serial Numbers

    97 of 97 codes

    • 82-1138
    • 82-1586
    • 82-2089
    • 82-2117
    • 82-2182
    • 82-2214
    • 82-2226
    • 82-2262
    • 82-2264
    • 82-2308
    • 82-2312
    • 82-2314
    • 82-2321
    • 82-2328
    • 82-2380
    • 82-2391
    • 82-2438
    • 82-2483
    • 82-2512
    • 82-2516
    • 82-2535
    • 82-2722
    • 82-2796
    • 82-2821
    • 82-2846
    • 82-2848
    • 82-3052
    • 82-3055
    • 82-3129
    • 82-3144
    • 82-3170
    • 82-3171
    • 82-3201
    • 82-3256
    • 82-3267
    • 82-3314
    • 82-3350
    • 82-3361
    • 82-3377
    • 82-3467
    • 82-3468
    • 82-3659
    • 82-3709
    • 82-3722
    • 82-3859
    • 82-7016-MH
    • 82-7022-MH
    • 82-7037-MH
    • 82-7055-MH
    • 82-7062-MH
    • 82-7080-MH
    • 82-7086-MH
    • 82-7105-MH
    • 82-7114-MH
    • 82-7124-MH
    • 82-7131-MH
    • 82-7133-MH
    • 82-7137-MH
    • 82-7141-MH
    • 82-7154-CMH
Amount recalled
149 units

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide

Why it was recalled

GE initiated a correction to the instructions/use due to the potential for erroneous auto injection of contrast dye.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 10, 2013 · Data as of Sep 19, 5:25 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.