FDA recall record

Perkinelmer Life Sciences Multiphor II Electrophoresis System GE HealthCare Product Number recall — FDA Z-2685-2017

Potential for electric shock in the case of a failure to install the grommets, supplied with the system.

Class IIclassification
Z-2685-2017official record ID
Jul 12, 2017report date

Recall record at a glance

Official recordZ-2685-2017
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmPerkinelmer Life Sciences, Inc.
Report dateJul 12, 2017
Recall initiation dateMay 15, 2017
Quantity241 instruments
LocationBoston, MA, United States

Official product description

Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D electrophoresis and electrophoretic transfer Note: The Multiphor II Electrophoresis System (Class I) is the platform used with the hemoglobin electrophoresis gel kit ( Class II) sold by PerkinElmer as the Resolve Hemoglobin Kit (K050709: Product code JJN). The RESOLVE Systems Hemoglobin kit (K050709) is designed to separate whole blood, cord blood or dried blood spot specimen for detection of normal and variant hemoglobins by isoelectric focusing.

Why the product was recalled

Potential for electric shock in the case of a failure to install the grommets, supplied with the system.

Distribution information

US Nationwide Distribution

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

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About this record

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