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ENCOR NEEDLE GUIDE INSERT 10G — recall 55905

Health Canada — Medical Devices · Canada · 2016-08-25 · Type III

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Agency: Health Canada — Medical Devices
Recall identifier: 55905
Date of alert: 2016-08-25
Country / jurisdiction: Canada
Risk level: Type III
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Bard is notifying customers that specific lots of Encor Needle Guide Insert 10G, may instead contain a smaller diameter (12G) insert. The 12G needle guide insert does not allow the larger 10G needle probe to pass through rendering the device unusable.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/encor-needle-guide-insert-10g

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ENCOR NEEDLE GUIDE INSERT 10G — recall 55905

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