Product Wiki · Recalls · Health Canada — Medical Devices

INTERTAN 11.5mm x 18cm 125D (2018-06-15) — recall 58115

Health Canada — Medical Devices · Canada · 2018-07-27 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58115
Date of alert
2018-07-27
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The device is recalled due to a laser mark labeling error. The 11.5mm nail was incorrectly laser marked as a 10mm nail.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/intertan-115mm-x-18cm-125d-201

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