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JBWARMER (2016-07-22)
- Starting date:
- July 22, 2016
- Posting date:
- August 5, 2016
- 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-59700
Affected products
A. JBWARMER
Reason
On 29-jun-2016, Stickman received a product complaint from the distributor against the JB warmer device for no visual evidence of CSA approved (electrical safety certification). On 30-jun-2016, it was confirmed by a Canadian electrical certifying body that the device must be certified and back certification of units in field will not be permitted without inspection.
Affected products
A. JBWARMER
Lot or serial number
no lot # issued for device
Model or catalog number
Not Applicable
Companies
- Manufacturer
-
STICKMAN INDUSTRIES INC.
39 ENTERPRISE DRIVE
ARUNDEL
04046
Maine
UNITED STATES