Reported Jan 20, 2016 · Terminated

Perkin Elmer WIZARD2 10-detector, 550 samples Product Code: 2470-0100, 3470-0100. The Wizard gamma counter is intended…

Perkinelmer

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: Perkinelmer · 940 Winter Street · Waltham, MA · 02451

Is this the product you have?

    • Perkin Elmer WIZARD2 10-detector
    • 550
  • samples Product Code2470-0100, 3470-0100. The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
Lot codes and dates
  • Model Number2470-0100
  • Serial Numbers
    • DG06106436
    • DG08118240
    • DG02106050
    • DG06106502
    • DG11118609
    • DG01128795
    • DG02117461
    • DG12118702
    • DG09106861
    • DG05117833
    • DG05117834
    • DG10107006
    • DG06106452
    • DG09118367
    • DG03106154
    • DG04129081
    • DG06106559
    • DG06117903
    • DG07106599
    • DG09106774
    • DG05106387
    • DG06106524
    • DG10106949
    • DG09118284
    • DG05117787
    • DG04117755
    • DG09106770
    • DG03106196
    • DG04129159
    • DG08118192
    • DG06106469
    • DG08118189
    • DG04129075
    • DG12107252
    • DG12118677
    • DG06117923
    • DG08106741
    • DG03106186
    • DG12118759
    • DG01117444
    • DG02106112
    • DG12107236
    • DG11107031
  • DG12107249 DG11118612 DG05117781 Model3470-0100 (1
  • unit) Serial NumberDG02128911
Amount recalled
47 units

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide

Why it was recalled

The content of the second #023 barcode ID label in the Barcode ID Label Binder is incorrect. The second barcode ID label #023 symbol incorrectly identifies as #024 when scanned. If measurement protocols have been programmed for both ID #023 and #024, the protocol associated with barcode ID #024 is executed. If the error is undetected, the Gamma Counter may produce erroneous results.

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 Aug 4, 2017 · Data as of Sep 19, 6:00 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.