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VACUETTE 4 ML FX SODIUM FLUORIDE / POTASSIUM OXAL (2016-04-26)
- Starting date:
- April 26, 2016
- Posting date:
- May 31, 2016
- 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-58674
Affected products
A. VACUETTE 4 ML FX SODIUM FLUORIDE / POTASSIUM OXAL
Reason
The 4 mL FX Sodium Fluoride/Potassium Oxalate tube may have no or low additive (Sodium Fluoride and Potassium Oxalate), which can effect analytical results for glucose and lactate.
Affected products
A. VACUETTE 4 ML FX SODIUM FLUORIDE / POTASSIUM OXAL
Lot or serial number
A151137L
Model or catalog number
454297
Companies
- Manufacturer
-
Greiner Bio One GmbH
Bad Haller Strasse 32
kremsmeunster
4550
AUSTRIA