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Health product recall

BD Vacutainer Buffered Sodium Citrate Blood Collection Tube

Starting date:
January 17, 2017
Posting date:
February 14, 2017
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-62198

Reason

After receiving a customer complaint reporting erroneous results, BD confirmed that a limited portion of the referenced lot was manufactured with approximately twice the expected amount of buffered sodium citrate additive, an anticoagulant.

Affected products

BD Vacutainer Buffered Sodium Citrate Blood Collection Tube

Lot or serial number

6090572

Model or catalog number

369714

Companies

Manufacturer

Becton Dickinson and Company

1 Becton Drive

Franklin Lakes

07417

New Jersey

UNITED STATES