Bosworth SuperPaste

Starting date:

November 7, 2016

Posting date:

June 3, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-61284

Last updated: 2019-06-03

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  Reason
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  Affected products

Reason

Kits included under this lot number contain accelerator which when mixed with the white paste may prevent setting within the anticipated time period.

Affected products