Reported Jan 20, 2016 · Terminated

Perkin Elmer ClWIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050. The Wizard2 gamma counter is…

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 ClWIZARD2 5-detector
    • 550
  • samples Product Code2470-0050, 3470-0050. The Wizard2 gamma counter is intended to detect and count gamma radiation emitted by clinical samples
Lot codes and dates
  • Model2470-0050
  • Serial Numbers
    • DG05106329
    • DG02117493
    • DG11107166
    • DG09106782
    • DG07118133
    • DG07118141
    • DG09106791
    • DG04117727
    • DG06118036
    • DG12107192
    • DG02106101
    • DG04106223
    • DG01128843
    • DG12107272
    • DG07118124
    • DG09106892
    • DG12118684
    • DG12118673
    • DG11107126
    • DG04117704
    • DG04117763
    • DG01117363
    • DG06106484
    • DG12107240
    • DG01128871
    • DG05117880
    • DG12118685
    • DG09118357
    • DG03106204
    • DG05106386
    • DG11107137
    • DG03106172
    • DG03106206
    • DG02106113
    • DG09106818
    • DG02106065
    • DG04106309
    • DG09106882
    • DG11118590
    • DG06106483
    • DG01117316
    • DG08118221
    • DG06117898
    • DG12107263
    • DG08118250
    • DG12118711
    • DG04117710
    • DG06106448
    • DG06106453
    • DG06106463
    • DG06117912
    • DG03106135
    • DG01117373
    • DG05117837
    • DG06106517
    • DG01128805
    • DG06117970
  • DG04106310 DG02117521 DG06106538 Model3470-0050 (2
  • units) Serial NumbersDG12118660 DG10118464
Amount recalled
62 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.