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Reliance Endoscope Processor (June 12, 2006)

Starting date:
June 12, 2006
Posting date:
August 21, 2006
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Product Safety
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-31653

Reason

The FD1 valve installed in some Reliance EPS processors contains a plunger seat and gasket made of an incorrect material.

Affected products

Reliance Endoscope Processor

Lot or serial number

Not applicable

Model or catalog number

MB31-0447, MB31-0448, MB33-0447

Companies

Manufacturer
Not Applicable