Health product recall

Thio med w/ dex, hem, vit k (10mL) (2018-08-13)

Starting date:
August 13, 2018
Posting date:
August 31, 2018
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-67622

Affected products

Thio med w/ dex, hem, vit k (10mL)

Reason

An internal technical investigation has confirmed that the above product, has intermittently failed performance testing during stability studies with various anaerobic microorganisms.

Affected products

Thio med w/ dex, hem, vit k (10mL)

Lot or serial number

258908

Model or catalog number

R07182

Companies
Manufacturer
Thermo Fisher Scientific Inc
12076 Santa Fe Trail Drive
Lenexa
66215
Kansas
UNITED STATES