Recall Z-1108-2017

PerkinElmer Life and Analytical Sciences, Wallac, OY · initiated January 5, 2017

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Spare Disk Remover Module; Product Number: 61001820 Intended for in vitro quantitative and qualitative determination of analytes in body fluids.

Codes / lots: N/A

Reason for recall

The firm became aware that the ball bushing axels are defective in the GSP instrument. During exposure to humid conditions, there is a risk that the axle material will corrode. Deterioration of the axle can be observed as deposits of corrosion on the defective axles. Ball bushing axles may corrode and corrosion particle may cause contamination in the wells or the corrosion will cause movement issues and possibly spillage and causing contamination of the plate wells.

FDA-determined cause: Component change control

Action taken

The recall was initiated on January 5, 2017 via email sent through the PerkinElmer Technical Support group located in Akron Ohio. Actions to be taken by user: 1. As instructed in the analyte specific kit inserts, the use of Kit Controls is required to assure the day-to-day validity of results. Patient results should only be reported if control results for the assay meet the laboratorys established criteria for acceptability. 2. If a movement error occurs customers will be directed to contact their local PerkinElmer field service representative. The movement error may indicate deterioration of the axle and therefore the use of the instrument should be avoided until field service personnel have inspected the status of the ball bushing axles or replaced affected ball bushing axles. Actions to be taken by the PerkinElmer: As a corrective action, PerkinElmer will replace the affected ball bushing axles in all the GSP instruments identified in this FSCA/Recall. The replacement may take place either as part of the initial installation activity before the instrument is used, scheduled periodic maintenance, or during a dedicated service visit. This field correction is considered as mandatory by the manufacturer. Customers will be contacted by PerkinElmer to arrange the field service visit.

Details

Recall number
Z-1108-2017
Initiated
January 5, 2017
Posted by FDA
January 27, 2017
Terminated
August 24, 2017
Product code
KHO – Fluorometer, For Clinical Use
Quantity
24 instruments and 3 spare disk remover modules
Distribution
MA, SC, TX, AL OUS: China, Mexico, Peru, Morocco, Italy, Finland, Ecuador, Brazil
Recalling firm
PerkinElmer Life and Analytical Sciences, Wallac, OY, Turku

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-1107-2017 Class IIGenetic Screening Processor (GSP); PerkinElmer Part Number= 2021-0010 Intended for in…The firm became aware that the ball bushing axels are defective in the GSP instrument. During exposure to… 01/05/2017Terminated