Reported Jan 20, 2016 · Terminated

Perkin Elmer WIZARD2 2-detector, 550 samples Product Code: 2470-0020 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 2-detector
    • 550
  • samples Product Code2470-0020 The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
Lot codes and dates
  • Serial Numbers
    • DG02117524
    • DG09118363
    • DG08118156
    • DG08118195
    • DG02128922
    • DG10118375
    • DG12107235
    • DG08118222
    • DG02117537
    • DG08118184
    • DG09106872
    • DG11107116
    • DG03117626
    • DG03117611
    • DG01117425
    • DG12107293
    • DG09118332
    • DG06106503
    • DG06118006
    • DG01128820
    • DG12118707
    • DG05106427
    • DG03106166
    • DG11118630
    • DG01117434
    • DG09106779
    • DG02117500
    • DG12118742
    • DG06106477
    • DG03106208
    • DG09106800
    • DG10106903
    • DG05117853
    • DG03117671
    • DG06106473
    • DG04117754
    • DG04117698
    • DG11118538
    • DG11118617
    • DG01117392
    • DG03117644
    • DG05117882
    • DG03117655
    • DG04117683
    • DG02106106
    • DG05106347
    • DG06118043
    • DG10118385
    • DG08106671
    • DG01128869
    • DG06118023
    • DG05106328
    • DG02117516
    • DG11107142
    • DG05106354
    • DG08118254
    • DG03106181
    • DG03106197
    • DG02117505
    • DG11107105
Amount recalled
60 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.