Product Wiki · Recalls · Health Canada — Medical Devices

ARCTICGEL PADS (FOR ARCTIC SUN 2000 & 5000 MODELS) (2017-11-07) — recall 57784

Health Canada — Medical Devices · Canada · 2017-11-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
57784
Date of alert
2017-11-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Bard has received complaints reporting that the hydrogel peeled away from pads during the removal of the release liner. The issue affects specific lots of ARCTICGEL pad kits and may result in the insufficient adhesion of the hydrogel to the pad. Product return is not required as part of the recall notification.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/arcticgel-pads-arctic-sun-2000

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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