Reported Jan 20, 2016 · Terminated

Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard gamma counter is intended to detect and…

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 1-detector
    • 550
  • samples Product Code2470-0010 The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
Lot codes and dates
  • Serial Numbers
    • DG06106539
    • DG12118720
    • DG07106646
    • DG12107250
    • DG12107281
    • DG03117619
    • DG11118605
    • DG01117400
    • DG12107202
    • DG01117401
    • DG06106449
    • DG03117666
    • DG05117791
    • DG06106454
    • DG03106180
    • DG11118637
    • DG07118121
    • DG07106598
    • DG11118633
    • DG06106520
    • DG03106137
    • DG07118111
    • DG02128888
    • DG08118247
    • DG06118014
    • DG01128790
    • DG12107207
    • DG07106637
    • DG01128876
    • DG04117764
    • DG01106035
    • DG12118780
    • DG05106342
    • DG01117399
    • DG06117909
    • DG06118011
    • DG09106846
    • DG11107146
    • DG12118694
    • DG08118217
    • DG02106084
    • DG04117690
    • DG05117838
    • DG09106799
    • DG04117735
    • DG03117548
    • DG01117362
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.