FDA (Devices) recall action 71380
The FDA (Devices) publishes a recall like this one as 7 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 7 pages.
Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
The agency’s own wording, quoted from the enforcement report.
The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.
Perkinelmer is recalling 53 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Perkinelmer is recalling 54 WIZARD2 gamma counters worldwide due to a barcode label error that may produce erroneous results.
Perkinelmer is recalling 53 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Perkinelmer is recalling 179 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Perkinelmer is recalling two WIZARD2 gamma counters due to a barcode label error that may produce erroneous results.
Perkinelmer is recalling 18 WIZARD2 gamma counters because a barcode label error may produce erroneous results.
Perkinelmer is recalling 63 WIZARD2 gamma counters worldwide due to a barcode label error that may produce erroneous results.