Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2685-2017 — 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 elect

U.S. FDA — Device Enforcement · United States · 2017-05-15 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2685-2017
Date of alert: 2017-05-15
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Perkinelmer Life Sciences, Inc.
Product category: device
Product type: Devices

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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