Perkin Elmer WIZARD2 Gamma Counter Recall Due to Barcode Label Error
Perkinelmer is recalling 47 WIZARD2 gamma counters because a barcode label error may cause the device to execute the wrong measurement protocol, potentially producing erroneous results.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II. The hazard involves potential erroneous results due to a labeling error, which fits the criteria for moderate severity involving low-risk contamination or minor labeling errors without reported injuries.
Plain-English summary
Perkinelmer is recalling 47 units of the WIZARD2 1-detector, 550 samples gamma counter (Product Code: 2470-0010). The recall is due to an error in the second #023 barcode ID label in the Barcode ID Label Binder. When scanned, this label incorrectly identifies as #024.
If measurement protocols have been programmed for both ID #023 and #024, the device will execute the protocol associated with barcode ID #024. If this error is undetected, the gamma counter may produce erroneous results. The affected units were distributed worldwide, including the US and numerous international locations.
Consumers and healthcare facilities should check their devices against the provided serial numbers. If a device is affected, they should contact Perkinelmer for instructions on how to proceed.
The recalled product
- Product
- Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard gamma counter is intended to detect and count gamma radiation emitted by clinical samples
- Manufacturer
- Perkinelmer
- Affected units
- 47
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 7 recalled by Perkinelmer under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 7 products in this recall →Related recalls
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