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Health product recall

Automate 2500 Family Recapper Module

Starting date:
May 31, 2017
Posting date:
July 17, 2017
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-63988

Reason

Beckman Coulter has identified there is a potential that a component on the recapper module did not have the required coating specified for that part.

Affected products

Automate 2500 Family Recapper Module

Lot or serial number

All lots

Model or catalog number

ODL20616

Companies

Manufacturer
Beckman Coulter Inc.
250 S. Kraemer Blvd.
Brea
92821
UNITED STATES