PerkinElmer Recalls
22 recalls on record · August 8, 2012 to December 28, 2016 · Medical Devices
Recalls by year
12
13
15
16
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
December 28, 2016Medical DevicesFDA
PerkinElmer, Inc recalls PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677. Used with the: JANUS AUTOMATED WORKSTATIO
Hazard: Defective tips have the potential to pipette/dispense volumes 50-100% lower than is specified for the tips.
December 21, 2016Medical DevicesFDA
PerkinElmer, Inc recalls Perkin Elmer RoboRack 25ul, Clear, Non-Conductive, Filter Tips, Pre-sterilized Item Number: 6000689. Supplied for us
Hazard: Filter Tips molded incorrectly and may not seal to the Varispan tip adaptor properly causing inaccurate aspiration and dispensing
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 1-detector,3", 1000 samples. Product Code: 2480-0010 The Wizard gamma counter is intended to dete
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 10-detector, 1000 samples. Product Code: 2470-0200, 3470-0200. The Wizard gamma counter is intend
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 5-detector, 1000 samples Product Code: 2470-0150, 3470-0150 The Wizard gamma counter is intended
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 10-detector, 550 samples Product Code: 2470-0100, 3470-0100. The Wizard gamma counter is intended
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer ClWIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050. The Wizard2 gamma counter is intend
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wizard gamma counter is intended to detect and
Hazard: 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.
January 20, 2016Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard gamma counter is intended to detect and
Hazard: 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.
July 29, 2015Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 1-detector,3", 1000 samples Product Code: 2480-0010 The Wizard¿" gamma counter is intended to d
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 10-detector, 1000 samples Product Code: 2470-0200, 3470-0200 The Wizard¿" gamma counter is inte
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 5-detector, 1 000 samples Product Code: 2470-0150, 3470-0150 The Wizard¿" gamma counter is inte
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 10-detector, 550 samples Product Code: 2470-0100, 3470-0100 The Wizard¿" gamma counter is inten
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls WIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050 The Wizard¿" gamma counter is intended to detect
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wizard¿" gamma counter is intended to detect and count g
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
July 29, 2015Medical DevicesFDA
Perkinelmer recalls Perkin Elmer WIZARD2 1-detector, 550 samples Product Code: 2470-0010 The Wizard¿" gamma counter is intended to detec
Hazard: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
January 23, 2013Medical DevicesFDA
Perkinelmer recalls Microplate, truncated V-bottomed lots included in the above listed products Product Number: 1380 5465. DBS
Hazard: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
January 23, 2013Medical DevicesFDA
Perkinelmer recalls DBS MICROPLATE, TRUNCATED V-BOTTOMED Product Number: 3033-0010
Hazard: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
January 23, 2013Medical DevicesFDA
Perkinelmer recalls NEONATAL TOTAL GALACTOSE KIT Product Numbers: 3029-0010, 3029-001B. This kit i
Hazard: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
January 23, 2013Medical DevicesFDA
Perkinelmer recalls NEOBASE NON-DERIVATIZED MSMS KIT Product Number: 3040-001U. This tandem mass spect
Hazard: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
January 23, 2013Medical DevicesFDA
Perkinelmer recalls NEOGRAM AMINO ACIDS AND ACYLCARNITINES TANDEM MASS SPECTROMETRY KIT Product Number: 3026-0030. This kit is intende
Hazard: Truncated V-Bottomed Microplate Wells used in assays contain defective wells.
August 8, 2012Medical DevicesFDA
Perkinelmer recalls Perkin Elmer Genetic Screening Processor (GSP) Product Code: 2021-0010 Product Usage: The GSP instrument is a fully
Hazard: Contamination from GSP Shaker unit results in decreased signal activity of assay measurements for Genetic Screening for Neonatal IRT, TSH and IRT