PerkinElmer, Inc. Recalls

Overview of recall records associated with PerkinElmer, Inc., including dates, categories and classifications where available.

2recall records

Dec 28, 2016latest record date

Dec 21, 2016earliest record date

Recall history in this database

Classification mix: Class II: 2.

Medical DeviceDec 28, 2016

PerkinElmer 20ul Clear RoboRack Tip, Pipette (Qty 960) Item Number: 6000677 recall — FDA Z-0780-2017

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

Class IIFDA: TerminatedPerkinElmer, Inc.

Medical DeviceDec 21, 2016

PerkinElmer Perkin Elmer RoboRack 25ul, Clear, Non-Conductive, Filter Tips, Pre-sterilized recall — FDA Z-0747-2017

Filter Tips molded incorrectly and may not seal to the Varispan tip adaptor properly causing inaccurate aspiration and dispensing

Class IIFDA: TerminatedPerkinElmer, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies PerkinElmer, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.