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Health product recall

IMUBIND Adamts13 ELISA and Auto Ab ELISA (2014-06-26)

Starting date:
June 26, 2014
Posting date:
July 7, 2014
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-40389

Recalled Products

A) IMUBIND Adamts13 ELISA

B) IMUBIND Adamts13 Auto Ab ELISA

Reason

The recall is the result of Sekisui Diagnostics shipping two unlicensed In Vitro diagnostic devices into Canada to one customer.

Affected products

A) IMUBIND Adamts13 ELISA

 

Lot or serial number

Lot 130530, Exp: 11/15/2014

Lot 140117, Exp: 04/30/2015

 

Model or catalog number

813

Companies
Manufacturer

Sekisui Diagnostics, LLC

500 West Ave.

Stamford

06902

Connecticut

UNITED STATES



B) IMUBIND Adamts13 Auto Ab ELISA

Lot or serial number

Lot 121024, Exp: 03/31/2014

Model or catalog number

814

Companies
Manufacturer

Sekisui Diagnostics, LLC

500 West Ave.

Stamford

06902

Connecticut

UNITED STATES