LEEP PRECISION GENERATOR (2021-09-23)

Starting date:

September 23, 2021

Posting date:

October 15, 2021

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-76655

Last updated:
2021-10-15

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  Reason
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  Affected products

Affected Products

LEEP PRECISION GENERATOR

Reason

Manufacturer has determined that the affected leep precision and Quantum 2000 generators have potential for COAG to fail during leep procedure resulting in patient bleeding and requiring additional medical care.

Affected products