Medical device recalls Moderate risk

PerkinElmer, Inc recalls PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677. Used with the: JANUS AUTOMATED WORKSTATION…

Recall date
October 13, 2016
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-0780-2017
FDA classification
Class II
Brand / firm
PerkinElmer, Inc
Sold / distributed
IA, MD, NY, WA Foreign: France, Germany, The Netherlands, Hungary, Singapore

Why it was recalled

Defective tips have the potential to pipette/dispense volumes 50-100% lower than is specified for the tips.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677. Used with the: JANUS AUTOMATED WORKSTATION Product Codes: AJS4001, AJM4001, AJI4001, AJL4001, AJS8001, AJM8001, AJI8001, AJL8001, AJM4G01, AJI4G01, AJL4G01, AJM8G01, AJI8G01, AJL8G01, AJM4M01, AJI4M01, AJL4M01, AJM8M01, AJI8M01, AJL8M01 NGS EXPRESS Product Codes: AJS4NGS

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