StemPro MSC SFM CTS (2019-06-27)

Starting date:

June 27, 2019

Posting date:

July 15, 2019

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-70429

Last updated: 2019-07-15

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  Reason
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  Affected products

Affected Products

StemPro MSC SFM CTS

Reason

On June 6th, 2019, Thermo Fisher Scientific was made aware that the supplier for TGF Beta (PeproTech) made a change to the cell line used for the creation of the raw material and subsequently this raw material has been used in the manufacturing of finished goods, TGF B1, has not been tested for Adventitious Agents.

Affected products