Health product recall

BriteBlade Pro Fiber Optic System (2019-09-12)

Starting date:
September 12, 2019
Posting date:
October 11, 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-71221



Last updated: 2019-10-11

Affected Products

A. BriteBlade Pro Single-Use Fiber Optic Mac 3

B. Laryngoscope BrightBlade Pro Fibre Optic - Miller 2

C. BritePro Solo Fibre Optic Laryngoscope Handle With Batteries and Blade

Reason

User reports received that the spring/washer/bearing components in the block of the laryngoscope blade being loose and separated from the device.

Affected products

A. BriteBlade Pro Single-Use Fiber Optic Mac 3

Lot or serial number
  • 181000113
  • 181100001
  • 181200005
Model or catalog number
  • 040-713U
Companies
Manufacturer

Flexicare Medical LTD.

Cynon Valley Business Park

Mountain Ash

CF45 4ER

UNITED KINGDOM


B. Laryngoscope BrightBlade Pro Fibre Optic - Miller 2

Lot or serial number
  • 181000115
Model or catalog number
  • 040-722U
Companies
Manufacturer

Flexicare Medical LTD.

Cynon Valley Business Park

Mountain Ash

CF45 4ER

UNITED KINGDOM


C. BritePro Solo Fibre Optic Laryngoscope Handle With Batteries and Blade

Lot or serial number
  • 180900072
  • 180900104
  • 181100097
  • 181200024
Model or catalog number
  • 040-333U
Companies
Manufacturer

Flexicare Medical LTD.

Cynon Valley Business Park

Mountain Ash

CF45 4ER

UNITED KINGDOM