Endoscopic Applicator (2019-09-23)

Starting date:

September 23, 2019

Posting date:

October 25, 2019

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-71371

Last updated: 2019-10-25

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  Reason
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  Affected products

Affected Products

Endoscopic Applicator

Reason

Baxter Canada made the decision to request return of certain cold chain orders due to the potential that the shipments may have gone outside of the validated pack-out parameters (pack-outs are validated for 2-8C for 48 hours).  Baxter Canada was notified on Friday Sep 20 by our 3PL shipping provider that there was a delay at the processing location, which may cause the shipments to be delivered past the 48 hour limit. The orders could not be stopped and went out for delivery Monday Sep 23.

Affected products